De novo COX2 mutation in a LHON family of Caucasian origin: implication for the role of mtDNA polymorphism in human pathology.

Autor: Zhadanov, Sergey I.1,2 zhadanov@sas.upenn.edu, Atamanov, Vasiliy V.3, Zhadanov, Nikolay I.4, Schurr, Theodore G.1
Zdroj: Journal of Human Genetics. Mar2006, Vol. 51 Issue 3, p161-170. 10p. 3 Diagrams, 2 Charts, 1 Graph.
Databáze: Academic Search Ultimate