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A Familial Phenotypic and Genetic Study of Mutations in PFN1 Associated with Amyotrophic Lateral Sclerosis 被引量:1

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摘要 Dear Editor,Amyotrophic lateral sclerosis(ALS)is a progressive and fatal neurodegenerative disease that prominently affects both upper and lower motor neurons.The prevalence of ALS has been estimated at 2.6-3.0 per 100,000 in Europe,5.2 per 100,000 in the USA,and 1.9-9.9 per 100,000 in Asia[1-3].ALS is classified as sporadic(sALS)or familial(fALS),but only 5%-10% of cases are identified as familial[4,5].
出处 《Neuroscience Bulletin》 SCIE CAS CSCD 2020年第2期174-178,共5页 神经科学通报(英文版)
基金 supported by the Key Program of the Natural Science Foundation of Guangdong Province,China(2017B030311015) Guangzhou Municipal People’s Livelihood Science and Technology Project(201803010085) the National Key R&D Program of China(2017YFC1310200).
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