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A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia. (2021)

First Author: Whittaker DE

Attributed to: MRC Centre for Neurodevelopmental Disorders funded by MRC

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