Open AccessWhole exome sequencing identifies deleterious rare variants in CCDC141 in familial self-limited delayed puberty
Author(s) -
T Saengkaew,
G Ruiz-Babot,
A David,
A Mancini,
K Mariniello,
Cabrera CP,
Barnes Mr,
L Dunkel,
L Guasti,
Howard SR
Publication year - 2022
Publication title -
yearbook of pediatric endocrinology
Language(s) - Uncategorized
Resource type - Journals
eISSN - 1662-4009
pISSN - 1662-3991
DOI - 10.1530/ey.19.7.1
Subject(s) - exome sequencing , genetics , exome , biology , computational biology , mutation , gene
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