Analysis of a naturally occurring mutation in sucrase-isomaltase: Glutamine 1098 is not essential for transport to the surface of COS-1 cells

Biochimica et Biophysica Acta - Molecular Basis of Disease

Volumn 1406, Issue 3, 1998, Pages 299-306

  Ouwendijk, Joke ^a   Peters, Wilma J M ^a   Te Morsche, René H M ^a   Van de Vorstenbosch, Rinske A ^a   Ginsel, Leo A ^a   Naim, Hassan Y ^b   Fransen, Jack A M ^a  

^a RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

^b UNIVERSITY OF VETERINARY MEDICINE HANNOVER   (Germany)

Author keywords

Accumulation; Congenital sucrase isomaltase deficiency; Golgi; Intestine; Proline; Protein folding

Indexed keywords

ALANINE; GLUTAMINE; LYSINE; OLIGO 1,6 GLUCOSIDASE; SUCRASE;

ANIMAL CELL; ARTICLE; CELL STRAIN COS1; ENZYME DEFICIENCY; IMMUNOFLUORESCENCE; IMMUNOFLUORESCENCE MICROSCOPY; IMMUNOPRECIPITATION; MUTAGENESIS; MUTATION; NONHUMAN; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANIMALS; BIOLOGICAL TRANSPORT; CELL MEMBRANE; COS CELLS; GLUTAMINE; HUMANS; MEMBRANE GLYCOPROTEINS; MICROSCOPY, FLUORESCENCE; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; MUTATION; PRECIPITIN TESTS; RABBITS; RATS; SUCRASE-ISOMALTASE COMPLEX; TRANSFECTION;

EID: 0031810056     PISSN: 09254439     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4439(98)00016-7     Document Type: Article

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