Next generation sequencing technologies in the genetic diagnosis of Congenital Myasthenic Syndrome

被引：0

作者：

Toepf, A. ^{[1
]}

Azuma, Y. ^{[1
]}

Gorokhova, S. ^{[2
]}

O'Connor, E. ^{[1
]}

Porter, A. ^{[1
]}

Lorenzoni, P. ^{[3
]}

McMacken, G. ^{[1
]}

Alrohaif, H. ^{[1
]}

Harris, E. ^{[1
]}

Mueller, J. ^{[1
]}

Chaouch, A. ^{[1
]}

Cox, D. ^{[1
]}

Evangelista, T. ^{[1
]}

MacArthur, D. ^{[4
]}

Magnusson, O. ^{[5
]}

Nicole, S. ^{[6
]}

Roos, A. ^{[1
]}

Senderek, J. ^{[7
]}

Bartoli, M. ^{[2
]}

Abicht, A. ^{[8
]}

Lochmueller, H.

机构：

[1] Newcastle Univ, John Walton Muscular Dystrophy Res Ctr, Newcastle Upon Tyne, Tyne & Wear, England

[2] Univ Aix Marseille, INSERM, Marseille, France

[3] UFPR, Neurol Hosp Clin, Curitiba, Parana, Brazil

[4] Massachusetts Gen Hosp, Analyt & Translat Genet Unit, Boston, MA 02114 USA

[5] deCODE Genet, Reykjavik, Iceland

[6] Sorbonne Univ, INSERM, Paris, France

[7] Ludwig Maximilians Univ Munchen, Friedrich Baur Inst, Munich, Germany

[8] Med Genet Ctr, Munich, Germany

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2018年 / 26卷

关键词：

D O I：

暂无

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：

P10.44D

引用

页码：442 / 442

页数：1

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