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Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosis
Author(s) -
Caixia Xu,
Caixia Xu
Publication year - 2021
Publication title -
human mutation
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.24155
Subject(s) - citation , idiopathic scoliosis , biology , scoliosis , genealogy , genetics , library science , history , computer science