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Volumn 17, Issue 4, 2001, Pages 353-
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Two polymorphic mutations (c2331A>C and IVS11+142insAGAAATTTTAAGTCTT) in the human peroxin 1 gene (PEX1).
a
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Author keywords
[No Author keywords available]
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Indexed keywords
MEMBRANE PROTEIN;
PEX1 PROTEIN, HUMAN;
ARTICLE;
CHROMOSOME 7;
DISORDERS OF PEROXISOMAL FUNCTIONS;
GENETIC POLYMORPHISM;
GENETICS;
HUMAN;
INTRON;
MOLECULAR GENETICS;
MUTATION;
NUCLEOTIDE SEQUENCE;
BASE SEQUENCE;
CHROMOSOMES, HUMAN, PAIR 7;
DNA MUTATIONAL ANALYSIS;
HUMANS;
INTRONS;
MEMBRANE PROTEINS;
MOLECULAR SEQUENCE DATA;
MUTATION;
PEROXISOMAL DISORDERS;
POLYMORPHISM, GENETIC;
MLCS;
MLOWN;
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EID: 0035318149
PISSN: None
EISSN: 10981004
Source Type: Journal
DOI: 10.1002/humu.40 Document Type: Article |
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Times cited : (2)
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References (0)
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