Literature DB >> 15761389

Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness.

Christina Zeitz1, Roberta Minotti, Silke Feil, Gábor Mátyás, Frans P M Cremers, Carel B Hoyng, Wolfgang Berger.   

Abstract

PURPOSE: To describe the clinical features and genetic analysis of eight X-linked congenital stationary night blindness (XLCSNB) Dutch patients.
METHODS: Electroretinogram (ERG) measurements were assessed in Dutch patients. Molecular genetic testing by denaturing high performance liquid chromatography (DHPLC), single stranded conformation polymorphism (SSCP) analysis, and direct sequencing of the CACNA1F and NYX genes were performed in the patients possessing a negative Schubert Bornschein ERG.
RESULTS: Molecular genetic testing of CACNA1F and NYX revealed three novel and two known CACNA1F sequence variants as well as two novel sequence alterations in the NYX gene. While one of the CACNA1F sequence variants (5756G>A, R1919H) has been previously described as a common polymorphism in Japanese families, we did not found this transition in 100 European control alleles.
CONCLUSIONS: In a pool of eight diagnosed XLCSNB patients, five showed a sequence variation in the CACNA1F and two in the NYX gene. In only one of the eight patients no sequence alteration could be detected. This might be explained by a mutation in other, as yet unidentified coding or regulatory sequences of NYX or CACNA1F or additional genes.

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Year:  2005        PMID: 15761389

Source DB:  PubMed          Journal:  Mol Vis        ISSN: 1090-0535            Impact factor:   2.367


  17 in total

1.  X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.

Authors:  R Jalkanen; M Mäntyjärvi; R Tobias; J Isosomppi; E-M Sankila; T Alitalo; N T Bech-Hansen
Journal:  J Med Genet       Date:  2006-02-27       Impact factor: 6.318

2.  Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.

Authors:  Christina Zeitz; Barbara Kloeckener-Gruissem; Ursula Forster; Susanne Kohl; István Magyar; Bernd Wissinger; Gábor Mátyás; François-Xavier Borruat; Daniel F Schorderet; Eberhart Zrenner; Francis L Munier; Wolfgang Berger
Journal:  Am J Hum Genet       Date:  2006-08-23       Impact factor: 11.025

3.  The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.

Authors:  Bo Chang; John R Heckenlively; Philippa R Bayley; Nicholas C Brecha; Muriel T Davisson; Norm L Hawes; Arlene A Hirano; Ronald E Hurd; Akihiro Ikeda; Britt A Johnson; Maureen A McCall; Catherine W Morgans; Steve Nusinowitz; Neal S Peachey; Dennis S Rice; Kirstan A Vessey; Ronald G Gregg
Journal:  Vis Neurosci       Date:  2006 Jan-Feb       Impact factor: 3.241

4.  CSNB1 in Chinese families associated with novel mutations in NYX.

Authors:  Xueshan Xiao; Xiaoyun Jia; Xiangming Guo; Shiqiang Li; Zhikuan Yang; Qingjiong Zhang
Journal:  J Hum Genet       Date:  2006-05-03       Impact factor: 3.172

5.  Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation.

Authors:  J Jason McAnany; Kenneth R Alexander; Nalin M Kumar; Hongyu Ying; Anastasios Anastasakis; Gerald A Fishman
Journal:  Ophthalmic Genet       Date:  2013-01-04       Impact factor: 1.803

6.  Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindness.

Authors:  Ronald G Gregg; Maarten Kamermans; Jan Klooster; Peter D Lukasiewicz; Neal S Peachey; Kirstan A Vessey; Maureen A McCall
Journal:  J Neurophysiol       Date:  2007-09-19       Impact factor: 2.714

7.  Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.

Authors:  Maria M van Genderen; Mieke M C Bijveld; Yvonne B Claassen; Ralph J Florijn; Jillian N Pearring; Francoise M Meire; Maureen A McCall; Frans C C Riemslag; Ronald G Gregg; Arthur A B Bergen; Maarten Kamermans
Journal:  Am J Hum Genet       Date:  2009-11-05       Impact factor: 11.025

8.  Ultrastructural localization of GPR179 and the impact of mutant forms on retinal function in CSNB1 patients and a mouse model.

Authors:  Jan Klooster; Maria M van Genderen; Minzhong Yu; Ralph J Florijn; Frans C C Riemslag; Arthur A B Bergen; Ronald G Gregg; Neal S Peachey; Maarten Kamermans
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-10-23       Impact factor: 4.799

Review 9.  Sequence features, structure, ligand interaction, and diseases in small leucine rich repeat proteoglycans.

Authors:  Norio Matsushima; Hiroki Miyashita; Robert H Kretsinger
Journal:  J Cell Commun Signal       Date:  2021-04-15       Impact factor: 5.782

10.  Sequence variations of GRM6 in patients with high myopia.

Authors:  Xiaoyu Xu; Shiqiang Li; Xueshan Xiao; Panfeng Wang; Xiangming Guo; Qingjiong Zhang
Journal:  Mol Vis       Date:  2009-10-19       Impact factor: 2.367

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