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Paper Report for: Carlton_2003_Nat.Genet_34_91

Reference

Title: Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT
Carlton VE, Harris BZ, Puffenberger EG, Batta AK, Knisely AS, Robinson DL, Strauss KA, Shneider BL, Lim WA and Bull LN <2 more author(s)>
Ref: Nat Genet, 34:91, 2003 : PubMed

        



Related information

Gene_Locus| human-BAAT
Mutation | M76V_human-BAAT,



Citations formats

Carlton VE, Harris BZ, Puffenberger EG, Batta AK, Knisely AS, Robinson DL, Strauss KA, Shneider BL, Lim WA, Salen G, Morton DH, Bull LN (2003)
Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT
Nat Genet 34: 91-6

Carlton VE, Harris BZ, Puffenberger EG, Batta AK, Knisely AS, Robinson DL, Strauss KA, Shneider BL, Lim WA, Salen G, Morton DH, Bull LN (2003)
Nat Genet 34: 91-6



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