Screening for REEP1 Mutations in 31 Chinese Hereditary Spastic Paraplegia Families

Ma, XR; He, J; Liu, XX; Fan, DS

Fan, DS (corresponding author), Peking Univ Third Hosp, Dept Neurol, Beijing, Peoples R China.; Fan, DS (corresponding author), Beijing Municipal Key Lab Biomarker & Translat Re, Beijing, Peoples R China.; Fan, DS (corresponding author), Peking Univ, Key Lab Neurosci, Natl Hlth Commiss, Minist Educ, Beijing, Peoples R China.

FRONTIERS IN NEUROLOGY, 2020; 11 ():

Abstract

Background: REEP1 is a common cause of autosomal dominant hereditary spastic paraplegia (HSP) but is rare in China. The pathological mechanism of REEP......

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