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Volumn 11, Issue 4, 1998, Pages 332-333
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Analysis of five mutations in 20 mucopolysaccharidois type 1 patients: high prevalence of the W402X mutation. Mutations in brief no. 121. Online.
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Author keywords
[No Author keywords available]
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Indexed keywords
TRYPTOPHAN;
ALLELE;
AMINO ACID SUBSTITUTION;
ARTICLE;
GENETICS;
HUMAN;
HURLER SYNDROME;
ITALY;
MUTATION;
NUCLEOTIDE SEQUENCE;
PHENOTYPE;
SPAIN;
ALLELES;
AMINO ACID SUBSTITUTION;
DNA MUTATIONAL ANALYSIS;
HUMANS;
ITALY;
MUCOPOLYSACCHARIDOSIS I;
MUTATION;
PHENOTYPE;
SPAIN;
TRYPTOPHAN;
MLCS;
MLOWN;
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EID: 0032249356
PISSN: 10597794
EISSN: None
Source Type: Journal
DOI: 10.1002/(sici)1098-1004(1998)11:4<332::aid-humu16>3.0.co;2-p Document Type: Article |
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Times cited : (28)
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References (0)
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