Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations-Reference-Cited by-同舟云学术

Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations

Published:2002-07 Issue:2 Volume:295 Page:342-347
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Fauser Sascha,Luberichs Janina,Besch Dorothea,Leo-Kottler Beate

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference34 articles.

1. A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy;Huoponen;Am. J. Hum. Genet.,1991

2. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy;Wallace;Science,1988

3. An ND-6 mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy;Johns;Biochem. Biophys. Res. Commun.,1992

4. Leber's hereditary optic neuropathy. New genetic considerations;Newman;Arch. Neurol.,1993

5. A simple salting out procedure for extracting DNA from human nucleated cells;Miller;Nucleic Acids Res.,1988

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