Related Experiment Video
Updated: Jul 6, 2026
03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittent
E Di Pierro1, V Besana, V Brancaleoni
1Department of Internal Medicine- University of Milan, Centro Anemie Congenite-Maggiore Policlinico, Mangiagalli and Regina Elena Hospital IRCCS. Via F.Sforza, 35 20122 Milan, Italy. elena.dipierro@unimi.it
Human Genetics
|March 20, 2008
Abstract
No abstract available in PubMed .
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