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Updated: Jun 5, 2025

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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Authors' Reply: Using VNtyper from Whole Exome Sequencing Data to Detect Pathogenic Variants in the MUC1 Gene
Ilias Bensouna1,2, Thomas Robert3,4, Xavier Vanhoye5
1Soins Intensifs Néphrologiques et Rein Aigu (SINRA), Nephrology Department, Tenon Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.
Journal of the American Society of Nephrology : JASN
|December 9, 2024
Abstract
No abstract available in PubMed .
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