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

被引：0
|
作者：
Yann Fichou
Nadia Bahi-Buisson
Juliette Nectoux
Jamel Chelly
Delphine Héron
Laurence Cuisset
Thierry Bienvenu
机构：
[1] Institut Cochin,
[2] Université Paris Descartes,undefined
[3] CNRS (UMR 8104),undefined
[4] Départment de Génétique et Développement,undefined
[5] Inserm,undefined
[6] U567,undefined
[7] Assistance Publique – Hôpitaux de Paris,undefined
[8] Hôpital Necker-Enfants Malades,undefined
[9] Service de Neuropédiatrie,undefined
[10] Assistance Publique – Hôpitaux de Paris,undefined
[11] Hôpital Cochin,undefined
[12] Laboratoire de Biochimie et Génétique Moléculaire,undefined
[13] Assistance Publique – Hôpitaux de Paris,undefined
[14] Hôpital Pitié-Salpétrière,undefined
[15] Service de Génétique Médicale,undefined
来源：
European Journal of Human Genetics | 2009年 / 17卷
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摘要：
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页码：1378 / 1380
页数：2
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