학술논문
Biallelic ATP2B1 variants as a likely cause of a novel neurodevelopmental malformation syndrome with primary hypoparathyroidism
Document Type
Article
Author
Source
In: European Journal of Human Genetics . (European Journal of Human Genetics, January 2024, 32(1):125-129)
Subject
Language
English
ISSN
14765438
10184813
10184813