Clinical and Genetic Heterogeneity of HCM: The Possible Role of a Deletion Involving MYH6 and MYH7
This case underscores the clinical and genetic heterogeneity of HCM, highlighting the importance of considering genomic deletions involving key sarcomeric genes in the diagnostic evaluation.
Authors
- Consolata Soddu (ORCID: https://orcid.org/0000-0002-4758-7801)
- S Murru (ORCID: https://orcid.org/0000-0003-0418-7223)
- Paola Neroni
- Salvatore Savasta (ORCID: https://orcid.org/0000-0001-9238-0749)
- Alessandra Coiana (ORCID: https://orcid.org/0000-0002-1039-5486)
- Giancarlo Mancuso
- Federica Incani (ORCID: https://orcid.org/0000-0003-2699-8035)
- Francesco Lai
- Milena Cau (ORCID: https://orcid.org/0000-0003-2652-0330)
- Marina Marsan
- Laura Serventi
Institutions
- University of Cagliari (IT)
- Ospedale Microcitemico (IT)
Publication Details
- Journal
- Genes
- Published
- 2025-02-10
- DOI
- https://doi.org/10.3390/genes16020212
- Citations
- 4
- Primary Topic
- Cardiomyopathy and Myosin Studies
- Type
- article
- Field-Weighted Citation Impact
- 5.55