z-logo
open-access-imgOpen Access
A Neonatal Case of Congenital Hyperinsulinism Due to Homozygous KCNJ11 Gene Mutation
Author(s) -
Hatice Demirol,
Özgür Olukman,
Özlem Nalbantoğlu Elmas,
Kıymet Çelik,
Rüya Çolak,
Şebnem Çalkavur
Publication year - 2017
Publication title -
the anatolian journal of general medical research
Language(s) - English
Resource type - Journals
eISSN - 1305-7146
pISSN - 1305-7073
DOI - 10.5222/terh.2017.163
Subject(s) - congenital hyperinsulinism , hyperinsulinism , mutation , genetics , medicine , gene , pediatrics , biology , insulin , insulin resistance

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom