Lack of association of common cystic fibrosis transmembrane conductance regulator gene mutations with primary sclerosing cholangitis. [electronic resource]
Producer: 20050429Description: 874-8 p. digitalISSN:- 0002-9270
- Adult
- Aged
- Alleles
- Biopsy
- Cholangitis, Sclerosing -- diagnosis
- Cystic Fibrosis -- diagnosis
- Cystic Fibrosis Transmembrane Conductance Regulator -- genetics
- DNA Mutational Analysis
- Female
- Gene Frequency -- genetics
- Genetic Variation
- Genotype
- Hepatitis C -- diagnosis
- Hepatitis, Autoimmune -- diagnosis
- Humans
- Liver -- pathology
- Male
- Middle Aged
- Phenotype
- Statistics as Topic
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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