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Paper Details

Whole exome sequencing identifies deleterious rare variants in CCDC141 in familial self-limited delayed puberty.
NPJ Genom Med
2
2021
Author NameAffiliation
Michael R BarnesWilliam Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London
Michael R BarnesNIHR Barts Cardiovascular Biomedical Research Centre, Barts and The London School of Medicine and Dentistry, Queen Mary University of London
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Release 1.2