Germline CDKN1B loss-of-function variants cause pediatric Cushing's disease with or without an MEN4 phenotype.
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F. Faucz | C. Stratakis | N. Pankratz | L. Hernández-Ramírez | J. Mills | D. Kay | P. Chittiboina | Denise M. Kay | J. Lane | M. Keil | F. Chasseloup | Tara Hussein Tayeb | Fanny Chasseloup