학술논문
A Founder Mutation in the POMC 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
Document Type
Article
Author
Source
In: Journal of Clinical Endocrinology and Metabolism . (Journal of Clinical Endocrinology and Metabolism, 1 September 2022, 107(9):E3654-E3660)
Subject
Language
English
ISSN
19457197
0021972X
0021972X