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Volumn 41, Issue 1, 1998, Pages 31-33
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An abnormal distribution of ΔF508 genotypes in cystic fibrosis patient registries
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Author keywords
F508 mutation; Cystic fibrosis; Distribution; Genotypes; Registries
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Indexed keywords
TRANSMEMBRANE CONDUCTANCE REGULATOR;
ALLELE;
ARTICLE;
CYSTIC FIBROSIS;
DISEASE SEVERITY;
GENE MUTATION;
GENOTYPE;
HUMAN;
MATHEMATICAL ANALYSIS;
MOLECULAR GENETICS;
REGISTER;
ADOLESCENT;
ADULT;
ALLELES;
CANADA;
CHILD;
CHILD, PRESCHOOL;
CYSTIC FIBROSIS;
CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;
FEMALE;
FRANCE;
GENE FREQUENCY;
GENOTYPE;
HUMANS;
INFANT;
INFANT, NEWBORN;
MALE;
MUTATION;
REGISTRIES;
SEQUENCE DELETION;
UNITED STATES;
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EID: 0031923652
PISSN: 00033995
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (3)
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References (7)
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