MECP2 mutation in a boy with language disorder and schizophrenia

被引：82

作者：

Cohen, D

Lazar, G

Couvert, P

Desportes, V

Lippe, D

Mazet, P

Héron, D

机构：

来源：

AMERICAN JOURNAL OF PSYCHIATRY | 2002年 / 159卷 / 01期

关键词：

D O I：

10.1176/appi.ajp.159.1.148-a

中图分类号：

R749 [精神病学];

学科分类号：

100205 ;

摘要：

引用

收藏

页码：148 / 149

页数：2

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[1] Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].

Amir, RE ;

Van den Veyver, IB ;

Wan, M ;

Tran, CQ ;

Francke, U ;

Zoghbi, HY .

NATURE GENETICS, 1999, 23 (02) :185-188

[2] Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males [J].

Clayton-Smith, J ;

Watson, P ;

Ramsden, S ;

Black, GCM .

LANCET, 2000, 356 (9232) :830-832

[3] MECP2 mutation in male patients with non-specific X-linked mental retardation [J].

Orrico, A ;

Lam, CW ;

Galli, L ;

Dotti, MT ;

Hayek, G ;

Tong, SF ;

Poon, PMK ;

Zappella, M ;

Federico, A ;

Sorrentino, V .

FEBS LETTERS, 2000, 481 (03) :285-288

[4] Rett syndrome and beyond:: Recurrent spontaneous and familial MECP2 mutations at CpG hotspots [J].

Wan, MM ;

Lee, SSJ ;

Zhang, XY ;

Houwink-Manville, I ;

Song, HR ;

Amir, RE ;

Budden, S ;

Naidu, S ;

Pereira, JLP ;

Lo, IFM ;

Zoghbi, HY ;

Schanen, NC ;

Francke, U .

AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (06) :1520-1529