MECP2 is highly mutated in X-linked mental retardation.

Couvert, P; Bienvenu, T; Aquaviva, C; Poirier, K; Moraine, C; Gendrot, C; Verloes, A; Andrès, C; Le Fevre, A C; Souville, I; Steffann, J; des Portes, V; Ropers, H H; Yntema, H G; Fryns, J P; Briault, S; Chelly, J; Cherif, B

Couvert, P; Bienvenu, T; Aquaviva, C; Poirier, K; Moraine, C; Gendrot, C; Verloes, A; Andrès, C; Le Fevre, A C; Souville, I; Steffann, J; des Portes, V; Ropers, H H; Yntema, H G; Fryns, J P; Briault, S; Chelly, J; Cherif, B.

Affiliation

Couvert P; INSERM Unité 129-ICGM, CHU Cochin 24 Rue du Faubourg Saint Jacques, 75014 Paris, France.

Hum Mol Genet ; 10(9): 941-6, 2001 Apr 15.

Article in En | MEDLINE | ID: mdl-11309367

Subject(s)

Chromosomal Proteins, Non-Histone; CpG Islands/genetics; DNA-Binding Proteins/genetics; Genetic Linkage; Intellectual Disability/genetics; Mutation; RNA-Binding Proteins; X Chromosome/genetics; Adult; Base Sequence; Female; Fragile X Mental Retardation Protein; Humans; Male; Methyl-CpG-Binding Protein 2; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins/genetics; Pedigree; Repressor Proteins/genetics; Rett Syndrome/genetics; Sex Factors

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Database: MEDLINE Main subject: X Chromosome / Chromosomal Proteins, Non-Histone / RNA-Binding Proteins / CpG Islands / DNA-Binding Proteins / Genetic Linkage / Intellectual Disability / Mutation Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Year: 2001 Type: Article

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