Glycoprotein lysosomal storage disorders: α- and β-mannosidosis, fucosidosis and α-N-acetylgalactosaminidase deficiency

Biochimica et Biophysica Acta - Molecular Basis of Disease

Volumn 1455, Issue 2-3, 1999, Pages 69-84

  Michalski, Jean Claude ^a   Klein, André ^b  

^a UNIVERSITÉ DES SCIENCES ET TECHNOLOGIES DE LILLE   (France)

^b LILLE UNIVERSITY HOSPITAL   (France)

Author keywords

N Acetylgalactosaminidase deficiency; Catabolism; Fucosidosis; Glycoprotein; Lysosomal storage disorder; Mannosidosis

Indexed keywords

ALPHA N ACETYLGALACTOSAMINIDASE; CARBOHYDRATE; GLYCAN; GLYCOPROTEIN; GLYCOSIDASE; LYSOSOME ENZYME; MONOSACCHARIDE;

ANIMAL MODEL; CLINICAL FEATURE; DISEASE COURSE; DISEASE SEVERITY; ENVIRONMENTAL FACTOR; ENZYME ACTIVITY; ENZYME DEFICIENCY; FUCOSIDOSIS; GENOTYPE; HUMAN; HYDROLYSIS; LYSOSOME STORAGE DISEASE; MANNOSIDOSIS; MUTATION; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; REVIEW;

ALPHA-MANNOSIDOSIS; ALPHA-N-ACETYLGALACTOSAMINIDASE; ANIMALS; CARBOHYDRATE SEQUENCE; CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME; DISEASE MODELS, ANIMAL; FUCOSIDOSIS; GLYCOSIDE HYDROLASES; HEXOSAMINIDASES; HUMANS; MOLECULAR SEQUENCE DATA; PHENOTYPE;

ANIMALIA;

EID: 0032860224     PISSN: 09254439     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4439(99)00077-0     Document Type: Review

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