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,...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
Main Authors: 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
Format: Artigo
Jezik:Inglês
Izdano: Korean Society for Biochemistry and Molecular Biology 2010
Teme:
Original Article
Online dostop: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
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki