Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system-Reference-Cited by-同舟云学术

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Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system

Published:2014-12 Issue:12 Volume:35 Page:2881.e11-2881.e15
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Liu Zhi-Jun,Li Hong-Fu,Tan Guo-He,Tao Qing-Qing,Ni Wang,Cheng Xue-Wen,Xiong Zhi-Qi,Wu Zhi-Ying

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference25 articles.

1. Clinical genetics of amyotrophic lateral sclerosis: what do we really know?;Andersen;Nat. Rev. Neurol.,2011

2. Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes;Andersen;Amyotroph. Lateral Scler. Other Motor Neuron Disord.,2003

3. Genetics of amyotrophic lateral sclerosis: an update;Chen;Mol. Neurodegener.,2013

4. Exome sequencing to identify de novo mutations in sporadic ALS trios;Chesi;Nat. Neurosci.,2013

5. First FDA authorization for next-generation sequencer;Collins;N. Engl. J. Med.,2013

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