𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson’s disease

✍ Scribed by Kenya Nishioka; Carles Vilariño-Güell; Stephanie A. Cobb; Jennifer M. Kachergus; Owen A. Ross; Emna Hentati; Faycal Hentati; Matthew J. Farrer


Book ID
116820857
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
146 KB
Volume
16
Category
Article
ISSN
1353-8020

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Mutant NDUFV2 subunit of mitochondrial c
✍ Paule Bénit; Réjane Beugnot; Dominique Chretien; Irina Giurgea; Pascale De Lonla 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 140 KB

Respiratory chain complex I deficiencies represent a genetically heterogeneous group of diseases resulting from mutations in either mitochondrial or nuclear DNA. Combination of denaturing high performance liquid chromatography and sequence analysis allowed us to show that a 4-bp deletion in intron 2