ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia

Genetics in Medicine

Volumn 13, Issue 10, 2011, Pages 891-894

  Glaser, Benjamin ^a   Blech, Ilana ^a   Krakinovsky, Yocheved ^b   Ekstein, Josef ^b   Gillis, David ^a   Mazor Aronovitch, Kineret ^c   Landau, Heddy ^c   Abeliovich, Dvorah ^a  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^b Dor Yeshorim   (Israel)

^c SHEBA MEDICAL CENTER   (Israel)

Author keywords

ABCC8; Ashkenazi Jews; Hyperinsulinemic hypoglycemia; SUR1

Indexed keywords

ABCC8 PROTEIN; INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.2; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; DATA BASE; FAMILY COUNSELING; FATHER CHILD RELATION; FEMALE; FOCAL HYPERINSULINEMIC HYPOGLYCEMIA; GENE FREQUENCY; GENE MUTATION; GENETIC RISK; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; GENOTYPE; HETEROZYGOSITY; HETEROZYGOSITY LOSS; HETEROZYGOTE; HUMAN; HYPERINSULINISM; HYPOGLYCEMIA; JEW; MAJOR CLINICAL STUDY; MALE; MUTATION; PANCREAS ISLET BETA CELL; PREGNANCY; PROGENY;

ATP-BINDING CASSETTE TRANSPORTERS; FEMALE; FOUNDER EFFECT; GENE FREQUENCY; GENETIC COUNSELING; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; GENOTYPE; HETEROZYGOTE; HUMANS; JEWS; PERSISTENT HYPERINSULINEMIA HYPOGLYCEMIA OF INFANCY; POINT MUTATION; POTASSIUM CHANNELS, INWARDLY RECTIFYING; PREGNANCY; RECEPTORS, DRUG; RISK FACTORS; SEQUENCE DELETION;

EID: 80053894221     PISSN: 10983600     EISSN: 15300366     Source Type: Journal    
DOI: 10.1097/GIM.0b013e31821fea33     Document Type: Article

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