Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities

Giri, D; Vignola, ML; Gualtieri, A; Scagliotti, V; McNamara, P; Peak, M; Didi, M; Gaston-Massuet, C; Senniappan, S

Senniappan, S (reprint author), Alder Hey Childrens Hosp NHS Fdn Trust, Dept Paediat Endocrinol, Eaton Rd, Liverpool, Merseyside, England.

HUMAN MOLECULAR GENETICS, 2017; 26 (22): 4315


Congenital hypopituitarism (CH) is characterized by the deficiency of one or more pituitary hormones and can present alone or in association with comp......

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