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Identification and Functional Analysis of a SLC33A1: c.339T > G (p.Ser113Arg) Variant in the Original SPG42 Family
2015-08-13  Hits:

Affiliation of Author(s):基础医学院
Journal:HUMAN MUTATION
Key Words:hereditary spastic paraplegias (HSP);exome sequencing;SLC33A1;mutation
First Author:毛飞
Document Code:1417758539073458177
Issue:0
Page Number:240-249
Number of Words:4
Translation or Not:no
Date of Publication:2015-08-13
Date of Publication:2015-08-13

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