Clinical phenotype and gene mutation analysis on one case of familial amyotrophic lateral sclerosis complicated with gastrocnemius edema caused by SOD1A4V

HOU Miao-miao; MAO Xiao-wei; LIU Wei; DING Yin-feng; ZHU Wen-hua; HOU Xiao-jun

doi:10.3969/j.issn.1672-6731.2019.06.009

Home>Articles>Clinical phenotype and gene mutation analysis on one case of familial amyotrophic lateral sclerosis complicated with gastrocnemius edema caused by SOD1A4V

DOI: 10.3969/j.issn.1672-6731.2019.06.009

Clinical phenotype and gene mutation analysis on one case of familial amyotrophic lateral sclerosis complicated with gastrocnemius edema caused by SOD1A4V

HOU Miao-miao

MAO Xiao-wei

LIU Wei

DING Yin-feng

ZHU Wen-hua

HOU Xiao-jun

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Publication Date：2019-01-01

Online Publishing Date：2025-08-15(First online date of this platform, not the publication date of the document)

Pages：6( 423-428 )

Chinese Journal of Contemporary Neurology and Neurosurgery

PKUISTIC

ISSN：1672-6731

Year, Vol.(Issue)：2019,19(6)