Diverse cardiac phenotypes among different carriers of the same MYH7 splicing variant allele (c.732+1G>A) from a family

BACKGROUND: Left ventricular non-compaction cardiomyopathy (LVNC) is a rare congenital heart defect. Gene defections have been found in patients with LVNC and their family members; and MYH7 is the most frequent gene associated with LVNC. METHODS: We performed a complete prenatal ultrasound and echoc...

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Detalles Bibliográficos
Autores principales: Tu, Peng, Sun, Hairui, Zhang, Xiaohang, Ran, Qian, He, Yihua, Ran, Suzhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8876400/
https://www.ncbi.nlm.nih.gov/pubmed/35209905
http://dx.doi.org/10.1186/s12920-022-01186-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8876400/
https://www.ncbi.nlm.nih.gov/pubmed/35209905
http://dx.doi.org/10.1186/s12920-022-01186-z

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