Heteroplasmy analysis in the Polish patients with 11778A mutation responsible for Leber hereditary optic neuropathy.

Mroczek-Tońska, Katarzyna

Heteroplasmy analysis in the Polish patients with 11778A mutation responsible for Leber hereditary optic neuropathy. [electronic resource] - Acta biochimica Polonica 2002 - 257-62 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0001-527X


Female
Heterozygote
Humans
Male
Mitochondria--genetics
Mutation
Optic Atrophy, Hereditary, Leber--genetics
Pedigree
Poland