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A Familial Phenotypic and Genetic Study of Mutations in PFN1 Associated with Amyotrophic Lateral Sclerosis.

Jieshan ChiJunling ChenYan LiZhiheng HuangLijuan WangLi-Juan Wang
Published in: Neuroscience bulletin (2019)
Keyphrases
  • amyotrophic lateral sclerosis
  • genome wide
  • copy number