Mutation in the SLC9A6 gene is not a frequent cause of sporadic Angelman-like syndrome

被引：12

作者：

Fichou, Yann ^{[1
,2
]}

Bahi-Buisson, Nadia ^{[3
]}

Nectoux, Juliette ^{[1
,2
]}

Chelly, Jamel ^{[1
,2
,4
]}

Heron, Delphine ^{[5
]}

Cuisset, Laurence ^{[1
,2
,4
]}

Bienvenu, Thierry ^{[1
,2
,4
]}

机构：

[1] Univ Paris 05, CNRS, UMR 8104, Inst Cochin,Dept Genet & Dev, Paris, France

[2] INSERM, U567, Paris, France

[3] Hop Necker Enfants Malad, Serv Neuropediat, AP HP, Paris, France

[4] Hop Cochin, AP HP, Lab Biochim & Genet Mol, F-75674 Paris, France

[5] Hop La Pitie Salpetriere, AP HP, Serv Genet Med, Paris, France

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2009年 / 17卷 / 11期

关键词：

DIAGNOSTIC-CRITERIA; MENTAL-RETARDATION; CONSENSUS; CHILDREN;

D O I：

10.1038/ejhg.2009.82

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：1378 / 1380

页数：3

共 11 条

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