Congenital sucrase-isomaltase deficiency: Heterogeneity of inheritance, trafficking, and function of an intestinal enzyme complex

Journal of Pediatric Gastroenterology and Nutrition

Volumn 55, Issue SUPPL.2, 2012, Pages

  Naim, Hassan Y ^a   Heine, Martin ^a   Zimmer, Klaus Peter ^b  

^a UNIVERSITY OF VETERINARY MEDICINE HANNOVER   (Germany)

^b JUSTUS LIEBIG UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLUCOSIDASE; ENDOPLASMIC RETICULUM GOLGI INTERMEDIATE COMPARTMENT PROTEIN 53; GLUCOSE; INTESTINE ENZYME; OLIGO 1,6 GLUCOSIDASE; SUCRASE; SUCRASE ISOMALTASE; SUCROSE;

AUTOSOMAL RECESSIVE DISORDER; BIOSYNTHESIS; CELL CYCLE ARREST; CELL FUNCTION; CELLULAR DISTRIBUTION; CONFERENCE PAPER; CONGENITAL SUCRASE ISOMALTASE DEFICIENCY; DIARRHEA; ENDOPLASMIC RETICULUM; ENZYME ACTIVITY; ENZYME DEFICIENCY; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC VARIABILITY; GLUCOSE BLOOD LEVEL; GOLGI COMPLEX; GROWTH RETARDATION; HUMAN; INHERITANCE; KIDNEY CALCIFICATION; MALABSORPTION; METABOLIC ACIDOSIS; MUSCLE HYPOTONIA; NEPHROLITHIASIS; PATHOGENESIS; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL; PROTEIN CLEAVAGE; PROTEIN DEGRADATION; PROTEIN FOLDING; PROTEIN PROCESSING; PROTEIN STRUCTURE; SACCHAROMYCES CEREVISIAE; STEATORRHEA; VOMITING;

CARBOHYDRATE METABOLISM, INBORN ERRORS; DIETARY CARBOHYDRATES; HUMANS; INTESTINAL MUCOSA; MUTATION; STARCH; SUCRASE-ISOMALTASE COMPLEX; SUCROSE;

EID: 84868666262     PISSN: 02772116     EISSN: 15364801     Source Type: Journal    
DOI: 10.1097/01.mpg.0000421402.57633.4b     Document Type: Conference Paper

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