Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis-Reference-Cited by-同舟云学术

Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis

Published:2002-04-30 Issue:5 Volume:51 Page:630-634
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Kim Ji Yeon,Hwang Jeong-Min,Park Sung Sup

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference19 articles.

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

2. Mitochondria and neuro-ophthalmologic diseases. In: eds. The metabolic and molecular bases of inherited disease. New York: McGraw-Hill, 2001: 2425-2509.

3. Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene

4. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy

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