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...

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Bibliographic Details
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
Format: Journal article
Language:English
Published: 2012

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