Revealing a New Homozygous Variant in CYP17A1 c.908G>A (p. Gly303Asp) by Genotyping a Chinese Patient with 46, XY 17a-Hydroxylase/17,20-Lyase Deficiency and Adrenal Space-Occupying Lesion
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Published:2024
Issue:184
Volume:36
Page:1012
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ISSN:1539-6509
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Container-title:Discovery Medicine
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language:en
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Short-container-title:Discovery Medicine
Author:
Wang Miao,Hu Xuejian,Xu Xiangyu,Chen Hui,Xue Jisu
Publisher
Discovery Medicine