Congenital glucose-galactose malabsorption: A novel deletion within the SLC5A1 gene

European Journal of Pediatrics

Volumn 172, Issue 3, 2013, Pages 409-411

  Vallaeys, L ^a   Van Biervliet, S ^b   De Bruyn, G ^a   Loeys, B ^c   Moring, A S ^d   Van Deynse, E ^d   Cornette, L ^a  

^a AZ Sint Jan Brugge Oostende AV ^*  (Belgium)

^b GHENT UNIVERSITY HOSPITAL   (Belgium)

^c ANTWERP UNIVERSITY HOSPITAL   (Belgium)

^d SINT AUGUSTINUS HOSPITAL   (Belgium)

Author keywords

Glucose galactose malabsorption; Neonatal diarrhoea; SLC5A1

Indexed keywords

GLUCOSE; REDUCING AGENT; SODIUM CHLORIDE; SODIUM GLUCOSE COTRANSPORTER 1;

ARTICLE; CASE REPORT; CHROMATOGRAPHY; CONGENITAL GLUCOSE GALACTOSE MALABSORPTION; DEHYDRATION; DIARRHEA; EXON; FEMALE; GENE DELETION; HUMAN; HYPERNATREMIA; IRRITABILITY; MALABSORPTION; MUTATIONAL ANALYSIS; NEWBORN; NEWBORN INTENSIVE CARE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEINURIA; REHYDRATION; WEIGHT REDUCTION;

BASE SEQUENCE; FEMALE; GALACTOSE; GENETIC MARKERS; GLUCOSE; HOMOZYGOTE; HUMANS; INFANT, NEWBORN; MALABSORPTION SYNDROMES; SEQUENCE DELETION; SODIUM-GLUCOSE TRANSPORTER 1;

EID: 84877156313     PISSN: 03406199     EISSN: 14321076     Source Type: Journal    
DOI: 10.1007/s00431-012-1802-9     Document Type: Article

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