Literature DB >> 15156359

Private SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) families from Turkey.

Andrea M Richter1, Riza Koksal Ozgul, Virginie C Poisson, Haluk Topaloglu.   

Abstract

We studied five families with pediatric-onset recessive spastic ataxia from Turkey. The clinical characteristics and linkage studies are compatible with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS). SACS mutations are responsible for ARSACS in Québec families. In four of the five families tested we detected new disease-causing mutations using automated sequencing of SACS. Our study raises to 12 the number of SACS mutations detected in ARSACS patients with origins around the Mediterranean basin.

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Year:  2004        PMID: 15156359     DOI: 10.1007/s10048-004-0179-y

Source DB:  PubMed          Journal:  Neurogenetics        ISSN: 1364-6745            Impact factor:   2.660


  16 in total

1.  Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families.

Authors:  K Gücüyener; K Ozgül; C Paternotte; H Erdem; J F Prud'homme; M Ozgüç; H Topaloğlu
Journal:  Neuropediatrics       Date:  2001-06       Impact factor: 1.947

2.  ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF.

Authors:  J C Engert; P Bérubé; J Mercier; C Doré; P Lepage; B Ge; J P Bouchard; J Mathieu; S B Melançon; M Schalling; E S Lander; K Morgan; T J Hudson; A Richter
Journal:  Nat Genet       Date:  2000-02       Impact factor: 38.330

Review 3.  HEPN: a common domain in bacterial drug resistance and human neurodegenerative proteins.

Authors:  Marcin Grynberg; Heidi Erlandsen; Adam Godzik
Journal:  Trends Biochem Sci       Date:  2003-05       Impact factor: 13.807

4.  ARSACS goes global.

Authors:  Christopher M Gomez
Journal:  Neurology       Date:  2004-01-13       Impact factor: 9.910

5.  Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11.

Authors:  A Richter; J D Rioux; J P Bouchard; J Mercier; J Mathieu; B Ge; J Poirier; D Julien; G Gyapay; J Weissenbach; T J Hudson; S B Melançon; K Morgan
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

6.  [Carlevoix-Saguenay type recessive spastic ataxia. A report of a Spanish case].

Authors:  I Pascual-Castroviejo; S I Pascual-Pascual; J Viaño; V Martínez
Journal:  Rev Neurol       Date:  2000 Jul 1-15       Impact factor: 0.870

7.  Hereditary disorders in Saguenay-Lac-St-Jean (Quebec, Canada).

Authors:  M De Braekeleer
Journal:  Hum Hered       Date:  1991       Impact factor: 0.444

8.  Autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Authors:  J P Bouchard; A Barbeau; R Bouchard; R W Bouchard
Journal:  Can J Neurol Sci       Date:  1978-02       Impact factor: 2.104

9.  Identification of a SACS gene missense mutation in ARSACS.

Authors:  T Ogawa; Y Takiyama; K Sakoe; K Mori; M Namekawa; H Shimazaki; I Nakano; M Nishizawa
Journal:  Neurology       Date:  2004-01-13       Impact factor: 9.910

10.  Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type.

Authors:  G S Grieco; A Malandrini; G Comanducci; V Leuzzi; M Valoppi; A Tessa; S Palmeri; L Benedetti; A Pierallini; S Gambelli; A Federico; F Pierelli; E Bertini; C Casali; F M Santorelli
Journal:  Neurology       Date:  2004-01-13       Impact factor: 9.910

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  22 in total

Review 1.  [Clinical details and genetics of recessive ataxias].

Authors:  C Zühlke; F Kreuz; K Bürk
Journal:  Nervenarzt       Date:  2011-04       Impact factor: 1.214

2.  Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia.

Authors:  Brent L Fogel; Ji Yong Lee; Jessica Lane; Amanda Wahnich; Sandy Chan; Alden Huang; Greg E Osborn; Eric Klein; Catherine Mamah; Susan Perlman; Daniel H Geschwind; Giovanni Coppola
Journal:  Mov Disord       Date:  2012-01-27       Impact factor: 10.338

3.  Sacsin-related ataxia caused by the novel nonsense mutation Arg4325X.

Authors:  Yoichi Yamamoto; Masayuki Nakamori; Kuni Konaka; Seiichi Nagano; Haruo Shimazaki; Yoshihisa Takiyama; Saburo Sakoda
Journal:  J Neurol       Date:  2006-08-29       Impact factor: 4.849

Review 4.  A novel homozygous SACS mutation identified by whole exome sequencing-genotype phenotype correlations of all published cases.

Authors:  Georgia Xiromerisiou; Katerina Dadouli; Chrysoula Marogianni; Antonios Provatas; Panagiotis Ntellas; Dimitrios Rikos; Pantelis Stathis; Despina Georgouli; Gedeon Loules; Maria Zamanakou; Georgios M Hadjigeorgiou
Journal:  J Mol Neurosci       Date:  2019-11-07       Impact factor: 3.444

5.  Structures of ubiquitin-like (Ubl) and Hsp90-like domains of sacsin provide insight into pathological mutations.

Authors:  Marie Ménade; Guennadi Kozlov; Jean-François Trempe; Harshit Pande; Solomon Shenker; Sihara Wickremasinghe; Xinlu Li; Hamed Hojjat; Marie-Josée Dicaire; Bernard Brais; Peter S McPherson; Michael J H Wong; Jason C Young; Kalle Gehring
Journal:  J Biol Chem       Date:  2018-06-26       Impact factor: 5.157

6.  Assessment of whole-brain white matter by DTI in autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Authors:  K K Oguz; G Haliloglu; C Temucin; R Gocmen; A C Has; K Doerschner; A Dolgun; M Alikasifoglu
Journal:  AJNR Am J Neuroradiol       Date:  2013-04-18       Impact factor: 3.825

7.  Sacsinopathies: sacsin-related ataxia.

Authors:  Yoshihisa Takiyama
Journal:  Cerebellum       Date:  2007-02-28       Impact factor: 3.847

8.  Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): novel compound heterozygous mutations in the SACS gene.

Authors:  S Kamada; S Okawa; T Imota; M Sugawara; I Toyoshima
Journal:  J Neurol       Date:  2008-05-19       Impact factor: 4.849

9.  An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss.

Authors:  Alessandra Terracciano; Carlo Casali; Gaetano S Grieco; Daniela Orteschi; Silvia Di Giandomenico; Laura Seminara; Roberto Di Fabio; Rosalba Carrozzo; Alessandro Simonati; Giovanni Stevanin; Marcella Zollino; Filippo M Santorelli
Journal:  Neurogenetics       Date:  2008-11-20       Impact factor: 2.660

10.  ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia.

Authors:  Sascha Vermeer; Rowdy P P Meijer; Benjamin J Pijl; Janneke Timmermans; Johannes R M Cruysberg; Maaike M Bos; Helenius J Schelhaas; Bart P C van de Warrenburg; Nine V A M Knoers; Hans Scheffer; Berry Kremer
Journal:  Neurogenetics       Date:  2008-05-09       Impact factor: 2.660

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