Whole exome sequencing identifies deleterious rare variants in CCDC141 in familial self-limited delayed puberty
Tansit Saengkaew(Prince of Songkla University), Sasha Howard(Queen Mary University of London), Leo Dunkel(Kuopio University Hospital), Claudia Cabrera(Queen Mary University of London), Katia Mariniello(Queen Mary University of London), Alessia David(William Harvey Research Institute), Leonardo Guasti(Queen Mary University of London), Alessandra Mancini(Brigham and Women's Hospital), Michael R. Barnes(GlaxoSmithKline (United Kingdom)), Gerard Ruiz‐Babot(Boston Children's Hospital)
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