NovelJARID1C/SMCX mutations in patients with X-linked mental retardation - Vigipallia

0 avis

NovelJARID1C/SMCX mutations in patients with X-linked mental retardation

Archive ouverte

Tzschach, Andreas | Lenzner, Steffen | Moser, Bettina | Reinhardt, Richard | Chelly, Jamel | Fryns, Jean-Pierre | Kleefstra, Tjitske | Raynaud, Martine | Turner, Gillian | Ropers, Hans-Hilger | Kuss, Andreas | Jensen, Lars Riff

Edité par CCSD ; Wiley -

International audience

Langue: en

Consulter en ligne

Consulter le document

Suggestions

Du même auteur

Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation

Archive ouverte | Jensen, Lars Riff | CCSD

International audience

X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11

Archive ouverte | Jensen, Lars Riff | CCSD

International audience

Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation

Archive ouverte | Kalscheuer, Vera | CCSD

International audience

Chargement des enrichissements...