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Whole exome sequencing identifies deleterious rare variants in CCDC141 in familial self-limited delayed puberty. (2021)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41525-021-00274-w

PubMed Identifier: 34930920

Publication URI: http://europepmc.org/abstract/MED/34930920

Type: Journal Article/Review

Volume: 6

Parent Publication: NPJ genomic medicine

Issue: 1

ISSN: 2056-7944