Whole-exome sequencing identifies a homozygous donor splice...

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Clinical Genetics 2017 / 04

Whole-exome sequencing identifies a homozygous donor splice site mutation in STAG3 that causes primary ovarian insufficiency

He, Wen-Bin, Banerjee, Santasree, Meng, Lan-Lan, Du, Juan, Gong, Fei, Huang, Hui, Zhang, Xin-Xin, Wang, Yan-Yan, Lu, Guang-Xiu, Lin, Ge, Tan, Yue-Qiu
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Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.13034
Date:
April, 2017
File:
PDF, 1.00 MB
english, 2017
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