A novel deletion variant in TRAPPC2 causes...

BMC Medical Genetics 2020 / 12 Vol. 21; Iss. 1

A novel deletion variant in TRAPPC2 causes spondyloepiphyseal dysplasia tarda in a five-generation Chinese family

Zhang, Cai, Du, Caiqi, Ye, Juan, Ye, Feng, Wang, Renfa, Luo, Xiaoping, Liang, Yan
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Volume:
21
Journal:
BMC Medical Genetics
DOI:
10.1186/s12881-020-01052-8
Date:
December, 2020
File:
PDF, 1.26 MB
2020
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