Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases

Mitochondrial diseases are clinically and genetically heterogeneous disorders, which make the exact diagnosis and classification difficult. The purpose of this study was to identify pathogenic mtDNA mutations in 61 Korean unrelated families (or isolated patients) with MELAS or MERRF. In particular,...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Choi, Byung-Ok, Hwang, Jung Hee, Cho, Eun Min, Jeong, Eun Hye, Hyun, Young Se, Jeon, Hyeon Jeong, Seong, Ki Min, Cho, Nam Soo, Chung, Ki Wha
Formato: Artigo
Lenguaje:Inglês
Publicado: Korean Society for Biochemistry and Molecular Biology 2010
Materias:
Original Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2892598/
https://ncbi.nlm.nih.gov/pubmed/20440095
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3858/emm.2010.42.6.046
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares