Related Experiment Video
Updated: Jun 7, 2026
03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Gene symbol: MAP2K1. Disease: Cardio-Facio-Cutaneous syndrome
1Hôpital Robert Debré, Service de Biochimie Génétique, Bd Sérurier, 48, 75019, Paris, France. helene.cave@rdb.aphp.fr
Human Genetics
|October 21, 2010
Abstract
No abstract available in PubMed .
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