Double homozygosity for mutations of AGL and SCN9A mimicking neurohepatopathy syndrome

被引：7

作者：

Ebermann, I. ^{[1
]}

Elsayed, S. M. ^{[3
,4
,5
]}

Abdel-Ghaffar, T. Y. ^{[4
,5
]}

Nuernberg, G. ^{[2
,6
]}

Nuernberg, P. ^{[2
]}

Elsobky, E. ^{[3
]}

Bolz, H. J. ^{[1
]}

机构：

[1] Univ Hosp Cologne, Inst Human Genet, Cologne Ctr Genom, D-50931 Cologne, Germany

[2] Univ Hosp Cologne, Inst Genet, D-50931 Cologne, Germany

[3] Ctr Med Genet, Cairo, Egypt

[4] Yassin Abdelghaffar Char Ctr Liver Dis & Res, Cairo, Egypt

[5] Ain Shams Univ, Childrens Hosp, Cairo, Egypt

[6] RZPD Deutsch Ressourcenzentrum Genomforsch GmbH, Berlin, Germany

来源：

NEUROLOGY | 2008年 / 70卷 / 24期

关键词：

D O I：

10.1212/01.wnl.0000314731.65875.5c

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：2343 / 2344

页数：2

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