𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients

✍ Scribed by A-Mei Zhang, Xiaoyun Jia, Xiangming Guo, Qingjiong Zhang, Yong-Gang Yao


Book ID
119905301
Publisher
BioMed Central
Year
2012
Tongue
English
Weight
487 KB
Volume
10
Category
Article
ISSN
1479-5876

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Mitochondrial DNA mutation in an Italian
✍ Carla Carducci; Vincenzo Leuzzi; Massimo Scuderi; Anna Maria Negri; Corrado Bala πŸ“‚ Article πŸ“… 1991 πŸ› Springer 🌐 English βš– 305 KB

Mitochondrial (mt) DNA from a Southern Italian family with Leber hereditary optic neuropathy was analyzed for the presence of the reported mutation at position 11778 of the ND4 subunit gene. The point mutation was found in mt DNA extracted from peripheral blood in all members of the family with the