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Functional consequences of a novel point mutation in the CYP21A2 gene identified in a Chinese Han patient with nonclassic 21-hydroxylase deficiency
Chu, Xiaojing, Ding, Hu, Cui, Guanglin, Xu, Yujun, Wang, Dao Wen, He, YebingVolume:
80
Language:
english
Journal:
Clinical Endocrinology
DOI:
10.1111/cen.12309
Date:
June, 2014
File:
PDF, 39 KB
english, 2014