TY  - GEN
AU  - Carlton,Victoria E H
AU  - Harris,Baruch Z
AU  - Puffenberger,Erik G
AU  - Batta,A K
AU  - Knisely,A S
AU  - Robinson,Donna L
AU  - Strauss,Kevin A
AU  - Shneider,Benjamin L
AU  - Lim,Wendell A
AU  - Salen,Gerald
AU  - Morton,D Holmes
AU  - Bull,Laura N
TI  - Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT
SN  - 1061-4036
PY  - 2003///0527
KW  - Acyltransferases
KW  - genetics
KW  - Bile Acids and Salts
KW  - blood
KW  - Case-Control Studies
KW  - Ethnicity
KW  - Female
KW  - Genotype
KW  - Humans
KW  - Linkage Disequilibrium
KW  - Liver
KW  - pathology
KW  - Malabsorption Syndromes
KW  - Male
KW  - Membrane Proteins
KW  - Mutation
KW  - Pedigree
KW  - Pennsylvania
KW  - Phenotype
KW  - Tight Junctions
KW  - Zonula Occludens-2 Protein
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1038/ng1147
ER  -