(PDF) A Human De Novo Mutation inMYH10phenocopies the Loss

A Human De Novo Mutation inMYH10phenocopies the Loss of Function Mutation in Mice

Rare Diseases

doi 10.4161/rdis.26144

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Abstract

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Date

January 1, 2013

Authors

Kelly DF Gonzalez

Publisher

Informa UK Limited

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