Abnormalities of hepatocyte nuclear factor (HNF)-1β: Biological mechanisms, phenotypes, and clinical consequences;Les anomalies de l'hepatocyte nuclear factor (HNF)-1β : mécanismes biologiques, phénotypes et conséquences cliniques

Archives de Pediatrie

Volumn 16, Issue 7, 2009, Pages 1049-1056

  Ulinski, T ^a   Bensman, A ^a   Lescure, S ^b  

^a ARMAND TROUSSEAU HOSPITAL   (France)

^b AP HP ^*  (France)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSE; HEPATOCYTE NUCLEAR FACTOR 1BETA;

CHILD HEALTH CARE; DIABETIC NEPHROPATHY; DIABETOGENESIS; DYSLIPIDEMIA; ECHOGRAPHY; EMBRYO DEVELOPMENT; FOLLOW UP; GENE DELETION; GENE EXPRESSION REGULATION; GENE MUTATION; GENETIC ASSOCIATION; GENOTYPE PHENOTYPE CORRELATION; GLUCOSE METABOLISM; GOUT; HEPATOBILIARY DISEASE; HUMAN; HYPERURICEMIA; HYPOMAGNESEMIA; KIDNEY CYST; KIDNEY DYSFUNCTION; KIDNEY DYSPLASIA; KIDNEY HYPOPLASIA; MATURITY ONSET DIABETES MELLITUS; MUTATIONAL ANALYSIS; NONHUMAN; PANCREAS DISEASE; PATHOPHYSIOLOGY; PHENOTYPIC VARIATION; PRENATAL DIAGNOSIS; PROTEIN ANALYSIS; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; SHORT SURVEY; UROGENITAL TRACT DISEASE;

CHILD; CHILD, PRESCHOOL; DIABETES MELLITUS, TYPE 2; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HEPATOCYTE NUCLEAR FACTOR 1-BETA; HUMANS; INFANT; INFANT, NEWBORN; KIDNEY; KIDNEY CORTEX; PHENOTYPE; POLYCYSTIC KIDNEY DISEASES; PREGNANCY; PROGNOSIS; ULTRASONOGRAPHY, PRENATAL;

EID: 67649336996     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.arcped.2009.02.023     Document Type: Short Survey

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