Novel PYGL mutations in Chinese children leading to...

Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reports

Luo, Xiaomei, Hu, Jiacheng, Gao, Xueren, Fan, Yanjie, Sun, Yu, Gu, Xuefan, Qiu, Wenjuan
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Volume:
21
Journal:
BMC Medical Genetics
DOI:
10.1186/s12881-020-01010-4
Date:
December, 2020
File:
PDF, 1.03 MB
2020
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