Aspartylglycosaminuria: Biochemistry and molecular biology

Biochimica et Biophysica Acta - Molecular Basis of Disease

Volumn 1455, Issue 2-3, 1999, Pages 139-154

  Aronson Jr , Nathan N ^a  

^a Dept Biochem Molec Biol U ^*  (United States)

Author keywords

Aspartylglucosaminuria; Aspartylglycosaminuria; Glycoprotein catabolism; Glycosylasparaginase; Lysosomal storage disease; N Terminal nucleophile amidase

Indexed keywords

AMIDASE; COMPLEMENTARY DNA; GLYCOPROTEIN; LEUKOCYTE ENZYME; N4 (BETA N ACETYLGLUCOSAMINYL)ASPARAGINASE; OLIGOSACCHARIDE;

ALLELE; AMINO TERMINAL SEQUENCE; ANIMAL MODEL; ASPARTYLGLYCOSAMINURIA; AUTOSOMAL RECESSIVE DISORDER; BIOCHEMISTRY; CRYSTAL STRUCTURE; DISEASE CARRIER; DISEASE COURSE; ENZYME ACTIVATION; ENZYME STRUCTURE; ENZYME SUBUNIT; FINLAND; GENE DELETION; GENE INSERTION; GENE MUTATION; GENE STRUCTURE; HUMAN; HYDROLYSIS; KNOCKOUT MOUSE; LYSOSOME STORAGE DISEASE; MISSENSE MUTATION; MOLECULAR BIOLOGY; MOUSE; NERVE CELL; NONHUMAN; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; POPULATION GENETIC PARAMETERS; PRIORITY JOURNAL; PROTEIN DEGRADATION; REVIEW;

ACETYLGLUCOSAMINE; AMINO ACID SEQUENCE; ANIMALS; ASPARTYLGLUCOSYLAMINASE; BASE SEQUENCE; DISEASE MODELS, ANIMAL; DNA, COMPLEMENTARY; EVOLUTION, MOLECULAR; FINLAND; GENE DELETION; GENE REARRANGEMENT; GLYCOPROTEINS; HUMANS; LYSOSOMAL STORAGE DISEASES; LYSOSOMES; MOLECULAR SEQUENCE DATA; MUTATION; MUTATION, MISSENSE;

EID: 0345035488     PISSN: 09254439     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4439(99)00076-9     Document Type: Review

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