Robert Wilson to Point Mutation
This is a "connection" page, showing publications Robert Wilson has written about Point Mutation.
Connection Strength
0.070
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A genetic defect resulting in mild low-renin hypertension. Proc Natl Acad Sci U S A. 1998 Aug 18; 95(17):10200-5.
Score: 0.038
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Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia. J Steroid Biochem Mol Biol. 2017 01; 165(Pt A):51-56.
Score: 0.032