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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Congenital Isolated ACTH Deficiency Caused by TBX19 Gene Mutation: A Family Report

Cheng Peng1, Guoyu Sun1, Zezhong Tang1

  • 1Department of Neonatal Ward, Peking University First Hospital, Beijing, China.

Frontiers in Pediatrics
|January 31, 2020
PubMed

Keywords:
ACTHCIADTBX19cholestasishypoglycemiaseizure

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