Variant Spectrum of Formin Homology 2 Domain‐Containing 3 Gene in Chinese Patients With Hypertrophic Cardiomyopathy

BACKGROUND: The FHOD3 (formin homology 2 domain‐containing 3) gene has recently been identified as a causative gene of hypertrophic cardiomyopathy (HCM). However, the pathogenicity of FHOD3 variants remains to be evaluated. This study analyzed the spectrum of FHOD3 variants in a large HCM and contro...

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Detalles Bibliográficos
Autores principales: Wu, Guixin, Ruan, Jieyun, Liu, Jie, Zhang, Channa, Kang, Lianming, Wang, Jizheng, Zou, Yubao, Song, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174292/
https://www.ncbi.nlm.nih.gov/pubmed/33586461
http://dx.doi.org/10.1161/JAHA.120.018236

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174292/
https://www.ncbi.nlm.nih.gov/pubmed/33586461
http://dx.doi.org/10.1161/JAHA.120.018236

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