학술논문
Molecular basis of CYP19A1 deficiency in a 46,XX patient with R550W mutation in POR: Expanding the PORD phenotype
Document Type
Article
Author
Source
In: Journal of Clinical Endocrinology and Metabolism . (Journal of Clinical Endocrinology and Metabolism, 1 April 2020, 105(4):E1272-E1290)
Subject
Language
English
ISSN
19457197
0021972X
0021972X