Literature DB >> 9541114

The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease.

F Meggouh1, A Benomar, H Rouger, S Tardieu, N Birouk, J Tassin, C Barhoumi, M Yahyaoui, T Chkili, A Brice, E LeGuern.   

Abstract

X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32). Using the SSCP technique and direct sequencing of PCR amplified genomic DNA fragments of the Cx32 gene from a Moroccan patient and her relatives, we identified the first de novo mutation of the Cx32 gene, consisting of a deletion of a G residue at position 499 in the Cx32 open reading frame. This previously unreported mutation produces a frameshift at position 147 in the protein and introduces a premature stop codon (TAG) at nucleotide 643, which results in the production of a truncated Cx32 molecule. This mutation illustrates the risk of an erroneous diagnosis of autosomal recessive CMT, especially in populations where consanguineous unions are frequent, and its consequences for genetic counselling, which can be avoided by molecular analysis.

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Year:  1998        PMID: 9541114      PMCID: PMC1051253          DOI: 10.1136/jmg.35.3.251

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  10 in total

1.  Hereditary motor and sensory neuropathy, X-linked: a half century follow-up.

Authors:  M P Rozear; M A Pericak-Vance; K Fischbeck; J M Stajich; P C Gaskell; D A Krendel; D G Graham; D V Dawson; A D Roses
Journal:  Neurology       Date:  1987-09       Impact factor: 9.910

2.  Genetic and clinical aspects of Charcot-Marie-Tooth's disease.

Authors:  H Skre
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

3.  Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13.

Authors:  V Timmerman; P De Jonghe; P Spoelders; S Simokovic; A Löfgren; E Nelis; J Vance; J J Martin; C Van Broeckhoven
Journal:  Neurology       Date:  1996-05       Impact factor: 9.910

4.  New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease.

Authors:  L J Bone; N Dahl; M W Lensch; P F Chance; T Kelly; E Le Guern; S Magi; G Parry; H Shapiro; S Wang
Journal:  Neurology       Date:  1995-10       Impact factor: 9.910

5.  Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families.

Authors:  H Rouger; E LeGuern; N Birouk; R Gouider; S Tardieu; E Plassart; M Gugenheim; J M Vallat; J P Louboutin; P Bouche; Y Agid; A Brice
Journal:  Hum Mutat       Date:  1997       Impact factor: 4.878

Review 6.  From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins.

Authors:  A E Harding
Journal:  Brain       Date:  1995-06       Impact factor: 13.501

7.  A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus.

Authors:  G Stevanin; E Le Guern; N Ravisé; H Chneiweiss; A Dürr; G Cancel; A Vignal; A L Boch; M Ruberg; C Penet
Journal:  Am J Hum Genet       Date:  1994-01       Impact factor: 11.025

8.  Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families.

Authors:  G Nicholson; J Nash
Journal:  Neurology       Date:  1993-12       Impact factor: 9.910

9.  Hereditary motor-sensory neuropathy (HMSN): possible X-linked dominant inheritance.

Authors:  L H Phillips; T E Kelly; P Schnatterly; D Parker
Journal:  Neurology       Date:  1985-04       Impact factor: 9.910

10.  Connexin mutations in X-linked Charcot-Marie-Tooth disease.

Authors:  J Bergoffen; S S Scherer; S Wang; M O Scott; L J Bone; D L Paul; K Chen; M W Lensch; P F Chance; K H Fischbeck
Journal:  Science       Date:  1993-12-24       Impact factor: 47.728

  10 in total
  4 in total

Review 1.  New evidence for secondary axonal degeneration in demyelinating neuropathies.

Authors:  Kathryn R Moss; Taylor S Bopp; Anna E Johnson; Ahmet Höke
Journal:  Neurosci Lett       Date:  2020-12-24       Impact factor: 3.046

2.  Segregation analysis in families with Charcot-Marie-Tooth disease allows reclassification of putative disease causing mutations.

Authors:  Rune Østern; Toril Fagerheim; Helene Hjellnes; Bjørn Nygård; Svein Ivar Mellgren; Øivind Nilssen
Journal:  BMC Med Genet       Date:  2014-01-21       Impact factor: 2.103

3.  A Cellular Assay for the Identification and Characterization of Connexin Gap Junction Modulators.

Authors:  Azeem Danish; Robin Gedschold; Sonja Hinz; Anke C Schiedel; Dominik Thimm; Peter Bedner; Christian Steinhäuser; Christa E Müller
Journal:  Int J Mol Sci       Date:  2021-01-31       Impact factor: 5.923

Review 4.  Current profile of Charcot-Marie-Tooth disease in Africa: A systematic review.

Authors:  Abdoulaye Yalcouyé; Kevin Esoh; Landouré Guida; Ambroise Wonkam
Journal:  J Peripher Nerv Syst       Date:  2022-04-05       Impact factor: 5.188

  4 in total

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