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Volumn 58, Issue 6, 1996, Pages 1127-1134
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Identification, expression, and biochemical characterization of N- acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patients
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Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENTARY DNA;
DNA;
N ACETYLGALACTOSAMINE 4 SULFATASE;
ANIMAL CELL;
ARTICLE;
CHO CELL;
CLINICAL ARTICLE;
CONTROLLED STUDY;
ENZYME DEFICIENCY;
HUMAN;
HUMAN CELL;
LYSOSOME STORAGE DISEASE;
MAROTEAUX LAMY SYNDROME;
MUCOPOLYSACCHARIDOSIS;
PHENOTYPE;
PRIORITY JOURNAL;
SITE DIRECTED MUTAGENESIS;
ADOLESCENT;
ANIMALS;
BASE SEQUENCE;
CHILD;
CHILD, PRESCHOOL;
CHO CELLS;
CHONDRO-4-SULFATASE;
CRICETINAE;
DNA PRIMERS;
DNA, COMPLEMENTARY;
HUMANS;
INFANT;
MOLECULAR SEQUENCE DATA;
MUCOPOLYSACCHARIDOSIS VI;
MUTAGENESIS, SITE-DIRECTED;
POINT MUTATION;
POLYMERASE CHAIN REACTION;
RECOMBINANT PROTEINS;
RESTRICTION MAPPING;
TRANSFECTION;
ANIMALIA;
CRICETINAE;
CRICETULUS GRISEUS;
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EID: 0029885020
PISSN: 00029297
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (56)
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References (0)
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