BENJAMIN SHNEIDER to Point Mutation
This is a "connection" page, showing publications BENJAMIN SHNEIDER has written about Point Mutation.
Connection Strength
0.111
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Inhibition of human m-epoxide hydrolase gene expression in a case of hypercholanemia. Biochim Biophys Acta. 2003 Jul 30; 1638(3):208-16.
Score: 0.049
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Novel fibrinogen gamma375 Arg-->Trp mutation (fibrinogen aguadilla) causes hepatic endoplasmic reticulum storage and hypofibrinogenemia. Hepatology. 2002 Sep; 36(3):652-8.
Score: 0.046
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Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: summary statement of a first National Institutes of Health/Office of Rare Diseases conference. J Pediatr. 2006 Aug; 149(2):159-64.
Score: 0.015