Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations.

Author:

Riordan-Eva P,Harding A E

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference65 articles.

1. Ein ungewohnlicher Fall von hereditare Amaurose;von Graefe A;Graefes Arch Ophthalmol

2. Ueber hereditare und congenital-angelegte Sehnervenleiden;Leber, T.;Graefes Arch Ophthalmol,1871

3. A probable case of cytoplasmic inheritance in man. A critique of Leber's disease. J7 Genet Hum 1936; 3;Imai, Y.; Moriwaki, D.

4. Leber's optic atrophy: a possible example of mitochondrial inheritance;Erikson, R.P.;Am Hum Genet,1972

5. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy;Wallace, D.C.; Singh, G.; Lott, M.T.;Science,1988

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