Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentations-Reference-Cited by-同舟云学术

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Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentations

Published:2002-01 Issue:1 Volume:51 Page:118-122
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Corona P.,Lamantea E.,Greco M.,Carrara F.,Agostino A.,Guidetti D.,Dotti M. T.,Mariotti C.,Zeviani M.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference19 articles.

1. Mitochondria and the heart

2. The genetics and pathology of oxidative phosphorylation

3. Mutations in mtDNA: Are We Scraping the Bottom of the Barrel?

4. Mitochondrial Disorders

5. Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho transformants

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