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

First Author: Whittaker DE
Attributed to:  The role of chromatin remodelling factors in cerebellar development and autism 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