Kevin Strauss to Malabsorption Syndromes
This is a "connection" page, showing publications Kevin Strauss has written about Malabsorption Syndromes.
Connection Strength
0.052
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Carlton VE, Harris BZ, Puffenberger EG, Batta AK, Knisely AS, Robinson DL, Strauss KA, Shneider BL, Lim WA, Salen G, Morton DH, Bull LN. Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. Nat Genet. 2003 May; 34(1):91-6.
Score: 0.052