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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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A case of Singleton-Merten syndrome without cardiac involvement harboring a novel IFIH1 variant
Jaime Vengoechea1, Janette DiMonda1
1Department of Human Genetics, Emory University, Atlanta, Georgia, USA.
American Journal of Medical Genetics. Part A
|March 24, 2020
Abstract
No abstract available in PubMed .
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