Volume 36, Issue. 2, February, 2020


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

 Jieshan Chi• Junling Chen1 • Yan Li1 • Zhiheng Huang1 • Lijuan Wang1 • Yuhu Zhang 1


1 Department of Neurology, Guangdong Neuroscience Institute, Guangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, China

 

Abstract 

 

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