Mitochondrial Genome Variants as a Cause of Mitochondrial Cardiomyopathy.

Campbell, Teresa; Slone, Jesse; Huang, Taosheng

Campbell, Teresa; Slone, Jesse; Huang, Taosheng.

Afiliación

Campbell T; Department of Pediatrics, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14203, USA.
Slone J; Department of Pediatrics, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14203, USA.
Huang T; Department of Pediatrics, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14203, USA.

Cells ; 11(18)2022 09 11.

Article en En | MEDLINE | ID: mdl-36139411

Asunto(s)

Cardiomiopatías; Genoma Mitocondrial; Enfermedades Mitocondriales; Adenosina Trifosfato; Calcio; Cardiomiopatías/genética; ADN Mitocondrial/genética; ADN Mitocondrial/metabolismo; Humanos; Enfermedades Mitocondriales/genética; Mutación; Especies Reactivas de Oxígeno

Palabras clave

calcium; dilated cardiomyopathy; ferroptosis; hypertrophic cardiomyopathy; iron overload; mitochondrial cardiomyopathy; mitochondrial genome; mtDNA; reactive oxygen species

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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales / Genoma Mitocondrial / Cardiomiopatías Idioma: En Revista: Cells Año: 2022 Tipo del documento: Article

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