Whole Mitochondrial Genome Analysis in Turkish Patients with Mitochondrial Diseases

BACKGROUND: Mitochondrial diseases are a clinically heterogeneous group of rare hereditary disorders that are defined by a genetic defect predominantly affecting mitochondrial oxidative phosphorylation. Mitochondrial diseases are caused by mutations of genes encoded by either nuclear DNA or mitochon...

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Detalles Bibliográficos
Autores principales: Gencer Öncül, Emine Begüm, Duman, Duygu, Eminoğlu, Fatma Tuba, Aktuna, Süleyman, Duman, Mustafa Türker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941229/
https://www.ncbi.nlm.nih.gov/pubmed/34928236
http://dx.doi.org/10.5152/balkanmedj.2021.21141

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941229/
https://www.ncbi.nlm.nih.gov/pubmed/34928236
http://dx.doi.org/10.5152/balkanmedj.2021.21141

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