Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes.
Defining the genetic contribution of rare variants to common diseases is a major basic and clinical science challenge that could offer new insights into disease etiology and provide potential for directed gene- and pathway-based prevention and treatment. Common and rare nonsynonymous variants in the...
Main Authors: | Rees, MG, Ng, D, Ruppert, S, Turner, C, Beer, N, Swift, A, Morken, M, Below, J, Blech, I, Mullikin, J, McCarthy, M, Biesecker, L, Gloyn, A, Collins, F |
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Format: | Journal article |
Language: | English |
Published: |
2012
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