Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy

Wabitsch, Martin; Lahr, G.; Van de Bunt, M.; Marchant, C.; Lindnert, M.; von Puttkamer, J.; Fenneberg, A.; Debatin, Klaus-Michael; Klein, R.; Ellard, S.; Clark, A.; Gloyn, A. L.

Erstveröffentlichung

2007

Metadata only
Search for full text

Wissenschaftlicher Artikel

Authors

Wabitsch, Martin

Lahr, G.

Van de Bunt, M.

Marchant, C.

Lindnert, M.

et al.

Institutions

UKU. Klinik für Kinder- und Jugendmedizin
UKU. Institut für Rechtsmedizin

Published in

Diabetic Medicine ; 24 (2007), 12. - S. 1393-1399. - ISSN 0742-3071

Link to publication

https://dx.doi.org/10.1111/j.1464-5491.2007.02285.x

Keywords

diazoxide; genetics; glucokinase; octreotide; persistent hyperinsulinaemic hypoglycaemia of infancy; glucokinase mutation; diabetes therapy; fasting glucose; birth-weight; gene; association; variants; kcnj11; a456v; mice

Dewey Decimal Group

DDC 610 / Medicine & health

Metadata

Show full item record