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 |
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Zdroj: | Journal of Human Genetics. Mar2006, Vol. 51 Issue 3, p161-170. 10p. 3 Diagrams, 2 Charts, 1 Graph. |
Databáze: | Academic Search Ultimate |
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