TY  - GEN
AU  - Flanagan,Sarah E
AU  - Patch,Ann-Marie
AU  - Locke,Jonathan M
AU  - Akcay,Teoman
AU  - Simsek,Enver
AU  - Alaei,Mohammadreza
AU  - Yekta,Zeinab
AU  - Desai,Meena
AU  - Kapoor,Ritika R
AU  - Hussain,Khalid
AU  - Ellard,Sian
TI  - Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigrees
SN  - 1945-7197
PY  - 2011///0523
KW  - 3-Hydroxyacyl CoA Dehydrogenases
KW  - genetics
KW  - Cohort Studies
KW  - Consanguinity
KW  - Diazoxide
KW  - Diuretics
KW  - Female
KW  - Genome-Wide Association Study
KW  - Haplotypes
KW  - Homozygote
KW  - Humans
KW  - Hyperinsulinism
KW  - Hypoglycemia
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Microsatellite Repeats
KW  - Mutation
KW  - physiology
KW  - Pedigree
KW  - Polymorphism, Single Nucleotide
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1210/jc.2010-1906
ER  -