The genétics of neonatal hyperinsulinism

Hormone Research

Volumn 59, Issue SUPPL. 1, 2003, Pages 30-34

  Fournet, Jean Christophe ^a   Junien, Claudine ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Cell KATP channel; Hyperinsulinism, congenital; Hypoglycaemia; Life threatening disease

Indexed keywords

ADENOSINE TRIPHOSPHATE; GLUCOKINASE; GLUTAMATE DEHYDROGENASE; INSULIN; POTASSIUM CHANNEL; PROTEIN SUBUNIT;

ALLELE; CHROMOSOME 11P; CONFERENCE PAPER; DEVELOPMENT; DISEASE ASSOCIATION; DISEASE SEVERITY; DOMINANT INHERITANCE; GENE CONTROL; GENE IDENTIFICATION; GENE MUTATION; GENETIC CODE; GENETIC COUNSELING; GENETIC HETEROGENEITY; GENETICS; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; HYPERAMMONEMIA; HYPERINSULINISM; HYPOGLYCEMIA; INSULIN RELEASE; MOLECULAR GENETICS; NEWBORN; PANCREAS; PANCREAS ISLET BETA CELL; PRIORITY JOURNAL; SYMPTOM; TREATMENT OUTCOME; CHEMISTRY; CHROMOSOME 11; CYTOLOGY; HETEROZYGOSITY LOSS; METABOLISM; MUTATION; PANCREAS ISLET; PATHOLOGY; REVIEW; SECRETION;

CHROMOSOMES, HUMAN, PAIR 11; GENETIC COUNSELING; GLUCOKINASE; GLUTAMATE DEHYDROGENASE; HUMANS; HYPERINSULINISM; INFANT, NEWBORN; INSULIN; ISLETS OF LANGERHANS; LOSS OF HETEROZYGOSITY; MUTATION; POTASSIUM CHANNELS;

EID: 0037269223     PISSN: 03010163     EISSN: None     Source Type: Journal    
DOI: 10.1159/000067842     Document Type: Conference Paper

References (20)

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