TY  - GEN
AU  - Wabitsch,M
AU  - Lahr,G
AU  - Van de Bunt,M
AU  - Marchant,C
AU  - Lindner,M
AU  - von Puttkamer,J
AU  - Fenneberg,A
AU  - Debatin,K M
AU  - Klein,R
AU  - Ellard,S
AU  - Clark,A
AU  - Gloyn,A L
TI  - Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy
SN  - 0742-3071
PY  - 2008///0416
KW  - Adolescent
KW  - Adult
KW  - Blood Glucose
KW  - analysis
KW  - Child
KW  - Congenital Hyperinsulinism
KW  - genetics
KW  - Family Health
KW  - Female
KW  - Glucokinase
KW  - Glucose Tolerance Test
KW  - Humans
KW  - Islets of Langerhans
KW  - enzymology
KW  - KATP Channels
KW  - Male
KW  - Middle Aged
KW  - Mutation, Missense
KW  - Pedigree
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1464-5491.2007.02285.x
ER  -