Fuch's corneal dystrophy in a patient with mitochondrial DNA mutations.

Author:

Albin R L

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference7 articles.

1. Oxidative phosphorylation diseases;Shoffner, J.M.; Wallace, D.C.,1995

2. A new manifestation of Leber's disease and a new explanation of the agency responsible for its unusual pattern of inheritence;Wallace, D.C.;Brain,1970

3. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation;Harding, A.E.; Sweeney, M.G.; Muller, D.H.;Brain,1992

4. Association of the 11778 mitochondrial DNA mutation and demyelinating disease;Neurology,1993

5. ATPase pump site density in human dysfunctional corneal endothelium;McCarmey, M.D.; Robertson, D.P.; Wood, T.O.; McLaughlin, B.J.;Invest Opthalmol Vis Sci,1987

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