Clinical and bi-genomic DNA findings of patients suspected to have mitochondrial diseases

Background: Mitochondrial diseases are the most common group of inherited metabolic disorders, causing difficulties in definite diagnosis due to clinical and genetic heterogeneity. Clinical components are predominantly associated with pathogenic variants shown in nuclear or mitochondrial genomes tha...

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Detalles Bibliográficos
Autores principales: Gedikbasi, Asuman, Toksoy, Guven, Karaca, Meryem, Gulec, Cagri, Balci, Mehmet Cihan, Gunes, Dilek, Gunes, Seda, Aslanger, Ayca Dilruba, Unverengil, Gokcen, Karaman, Birsen, Basaran, Seher, Demirkol, Mubeccel, Gokcay, Gulden Fatma, Uyguner, Zehra Oya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10292751/
https://www.ncbi.nlm.nih.gov/pubmed/37377599
http://dx.doi.org/10.3389/fgene.2023.1191159

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10292751/
https://www.ncbi.nlm.nih.gov/pubmed/37377599
http://dx.doi.org/10.3389/fgene.2023.1191159

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