Heterozygous deletions in MKRN3 cause central precocious puberty without Prader-Willi Syndrome
Meader, Brooke N, Albano, Alessandro, Sekizkardes, Hilal, Delaney, AngelaJournal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/clinem/dgaa331
Date:
June, 2020
File:
PDF, 702 KB
2020