Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death

BACKGROUND: Patients with some mutations in the lamin A/C (LMNA) gene are characterized by the presence of dilated cardiomyopathy (DCM), conduction abnormalities, ventricular tachyarrhythmias (VT), and sudden cardiac death (SCD). Various clinical features have been observed among patients who have t...

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Detalles Bibliográficos
Autores principales: Yokokawa, Tetsuro, Ichimura, Shohei, Hijioka, Naoko, Kaneshiro, Takashi, Yoshihisa, Akiomi, Kunii, Hiroyuki, Nakazato, Kazuhiko, Ishida, Takafumi, Suzuki, Osamu, Ohno, Seiko, Aiba, Takeshi, Ohtani, Hiroshi, Takeishi, Yasuchika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918565/
https://www.ncbi.nlm.nih.gov/pubmed/31847799
http://dx.doi.org/10.1186/s12872-019-01282-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918565/
https://www.ncbi.nlm.nih.gov/pubmed/31847799
http://dx.doi.org/10.1186/s12872-019-01282-6

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