A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia. (2021)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1172/jci141587
PubMed Identifier: 34730112
Publication URI: http://europepmc.org/abstract/MED/34730112
Type: Journal Article/Review
Volume: 131
Parent Publication: The Journal of clinical investigation
Issue: 24
ISSN: 0021-9738