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Mutation spectrum of Chinese patients with familial and sporadic amyotrophic lateral sclerosis

Authors

  • Qing Liu Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China Neuroscience Center, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS), Beijing, China PubMed articlesGoogle scholar articles
  • Fang Liu Neuroscience Center, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS), Beijing, China McKusick-Zhang Center for Genetic Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China PubMed articlesGoogle scholar articles
  • Bo Cui Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China Neuroscience Center, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS), Beijing, China PubMed articlesGoogle scholar articles
  • Chao Xia Lu Neuroscience Center, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS), Beijing, China McKusick-Zhang Center for Genetic Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China PubMed articlesGoogle scholar articles
  • Xia Nan Guo Neuroscience Center, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS), Beijing, China McKusick-Zhang Center for Genetic Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China PubMed articlesGoogle scholar articles
  • Rong Rong Wang Neuroscience Center, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS), Beijing, China McKusick-Zhang Center for Genetic Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China PubMed articlesGoogle scholar articles
  • Ming Sheng Liu Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China Neuroscience Center, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS), Beijing, China PubMed articlesGoogle scholar articles
  • Xiao Guang Li Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China Neuroscience Center, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS), Beijing, China PubMed articlesGoogle scholar articles
  • Li-ying Cui Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China Neuroscience Center, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS), Beijing, China PubMed articlesGoogle scholar articles
  • Xue Zhang Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China Neuroscience Center, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS), Beijing, China McKusick-Zhang Center for Genetic Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Xue Zhang, McKusick-Zhang Center for Genetic Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100005, China; xuezhang{at}pumc.edu.cnProfessor Li-ying Cui, Department of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100005, China; pumchcuily{at}sina.comQL and FL contributed equally.
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Citation

Liu Q, Liu F, Cui B, et al
Mutation spectrum of Chinese patients with familial and sporadic amyotrophic lateral sclerosis

Publication history

  • Received February 15, 2016
  • Revised May 17, 2016
  • Accepted May 31, 2016
  • First published June 16, 2016.
Online issue publication 
October 13, 2016

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