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Volumn 100, Issue 3, 1997, Pages
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A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotype.
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Author keywords
[No Author keywords available]
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Indexed keywords
CFTR PROTEIN, HUMAN;
CHLORIDE;
TRANSMEMBRANE CONDUCTANCE REGULATOR;
ARTICLE;
CHEMISTRY;
CHILD;
CLASSIFICATION;
CYSTIC FIBROSIS;
FEMALE;
FORCED EXPIRATORY VOLUME;
GENETIC TRANSCRIPTION;
GENETIC VARIABILITY;
GENETICS;
GENOTYPE;
HOSPITALIZATION;
HUMAN;
INFANT;
MALE;
MUTATION;
NUCLEAR FAMILY;
NUCLEOTIDE SEQUENCE;
ONSET AGE;
PANCREAS;
PATHOPHYSIOLOGY;
PHENOTYPE;
SWEAT;
AGE OF ONSET;
CHILD;
CHLORIDES;
CYSTIC FIBROSIS;
CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;
DNA MUTATIONAL ANALYSIS;
FEMALE;
FORCED EXPIRATORY VOLUME;
GENOTYPE;
HUMANS;
INFANT;
MALE;
MUTATION;
NUCLEAR FAMILY;
PANCREAS;
PHENOTYPE;
SEVERITY OF ILLNESS INDEX;
SWEAT;
TRANSCRIPTION, GENETIC;
VARIATION (GENETICS);
MLCS;
MLOWN;
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EID: 0031219150
PISSN: None
EISSN: 10984275
Source Type: Journal
DOI: 10.1542/peds.100.3.e5 Document Type: Article |
Times cited : (22)
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References (0)
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