Whole exome sequencing identifies deleterious rare variants in CCDC141 in familial self-limited delayed puberty (2021)
Abstract
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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
Parent Publication: npj Genomic Medicine
Issue: 1
ISSN: 2056-7944