Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. [electronic resource]
Producer: 20030527Description: 91-6 p. digitalISSN:- 1061-4036
- Acyltransferases -- genetics
- Bile Acids and Salts -- blood
- Case-Control Studies
- Ethnicity -- genetics
- Female
- Genotype
- Humans
- Linkage Disequilibrium
- Liver -- pathology
- Malabsorption Syndromes -- blood
- Male
- Membrane Proteins -- genetics
- Mutation
- Pedigree
- Pennsylvania
- Phenotype
- Tight Junctions -- pathology
- Zonula Occludens-2 Protein
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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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