Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French population.

Latour, P; Lévy, N; Paret, M; Chapon, F; Chazot, G; Clavelou, P; Couratier, P; Dumas, R; Ollagnon, E; Pouget, J; Setiey, A; Vallat, J M; Boucherat, M; Fontes, M; Vandenberghe, A

Latour, P; Lévy, N; Paret, M; Chapon, F; Chazot, G; Clavelou, P; Couratier, P; Dumas, R; Ollagnon, E; Pouget, J; Setiey, A; Vallat, J M; Boucherat, M; Fontes, M; Vandenberghe, A.

Affiliation

Latour P; Unité Neurogénétique Moléculaire, Hospices Civils de Lyon, Hôpital de l'Antiquaille, France.

Neurogenetics ; 1(2): 117-23, 1997 Sep.

Article in En | MEDLINE | ID: mdl-10732813

Subject(s)

Charcot-Marie-Tooth Disease/genetics; Connexins/genetics; X Chromosome/genetics; Adolescent; Adult; Aged; Amino Acid Substitution; Charcot-Marie-Tooth Disease/physiopathology; Child; DNA/chemistry; DNA/genetics; DNA Mutational Analysis; Demyelinating Diseases/genetics; Family Health; Female; France; Genetic Linkage; Humans; Male; Median Nerve/physiopathology; Middle Aged; Mutation; Pedigree; Point Mutation; Polymorphism, Single-Stranded Conformational; Sequence Deletion; Gap Junction beta-1 Protein

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Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Charcot-Marie-Tooth Disease / Connexins Limits: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Neurogenetics Journal subject: GENETICA / NEUROLOGIA Year: 1997 Type: Article Affiliation country: France

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