✦ LIBER ✦

Relative fitness of carriers of the mitochondrial DNA mutation 3243A > G

✍ Scribed by Moilanen, Jukka S; Majamaa, Kari

Book ID: 110025044
Publisher: Nature Publishing Group
Year: 2001
Tongue: English
Weight: 51 KB
Volume: 9
Category: Article
ISSN: 1018-4813
DOI: 10.1038/sj.ejhg.5200550

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Manifestations of the mitochondrial A324

Manifestations of the mitochondrial A3243G mutation

✍ Josef Finsterer 📂 Article 📅 2009 🏛 Elsevier Science 🌐 English ⚖ 66 KB

The mitochondrial DNA A3243G mutation in

The mitochondrial DNA A3243G mutation in Werner's syndrome

✍ Fujio Takeuchi; Shinji Harihara; Kenichi Nakamura; Kaiyo Takubo; Masao Kanamori; 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 78 KB

Prognosis of symptomatic patients with t

Prognosis of symptomatic patients with the A3243G mutation of mitochondrial DNA

✍ Liu, Chi-Hung; Chang, Chien-Hung; Kuo, Hung-Chou; Ro, Long-Sun; Liou, Chia-Wei; 📂 Article 📅 2012 🏛 Chinese Electronic Periodical Services 🌐 English ⚖ 262 KB

Clinical features of A3243G mitochondria

Clinical features of A3243G mitochondrial tRNA mutation

✍ Jong Hee Chae; Hee Hwang; Byung Chan Lim; Hae Il Cheong; Yong Seung Hwang; Ki Jo 📂 Article 📅 2004 🏛 Elsevier Science 🌐 English ⚖ 91 KB

Noninvasive diagnosis of the 3243A>G mit

Noninvasive diagnosis of the 3243A>G mitochondrial DNA mutation using urinary epithelial cells

✍ McDonnell, Martina T; Schaefer, Andrew M; Blakely, Emma L; McFarland, Robert; Ch 📂 Article 📅 2004 🏛 Nature Publishing Group 🌐 English ⚖ 92 KB

Prevalence, segregation, and phenotype o

Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children

✍ Johanna Uusimaa; Jukka S. Moilanen; Leena Vainionpää; Päivi Tapanainen; Päivi Li 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 212 KB 👁 2 views

## Abstract ## Objective We studied the prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children in a defined population in Northern Ostrobothnia, Finland. ## Methods Children with diagnoses commonly associated with mitochondrial diseases were ascertained. Blo