mtDNA Deletion in a Patient with Symptoms of Mitochondrial Cytopathy but without Ragged Red Fibers-Reference-Cited by-同舟云学术

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mtDNA Deletion in a Patient with Symptoms of Mitochondrial Cytopathy but without Ragged Red Fibers

Published:1995-10 Issue:1 Volume:56 Page:26-30
ISSN:1077-3150
Container-title:Biochemical and Molecular Medicine
language:en
Short-container-title:Biochemical and Molecular Medicine

Author:

Blok R.B.,Thorburn D.R.,Danks D.M.,Dahl H.H.M.

Publisher

Elsevier BV

Subject

Biochemistry

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical and molecular features of adPEO due to mutations in the Twinkle gene;Journal of the Neurological Sciences;2002-09

2. An Introduction: Oxidative Phosphorylation Diseases;Seminars in Neurology;2001

3. Skewed Segregation of the mtDNA nt 8993 (TrG) Mutation in Human Oocytes;The American Journal of Human Genetics;1997-06

4. Sporadic heteroplasmic single 5.5 Kb mitochondrial DNA deletion associated with cerebellar ataxia, hypogonadotropic hypogonadism, choroidal dystrophy, and mitochondrial respiratory chain complex I deficiency;Human Mutation;1997

5. Leigh syndrome: Clinical features and biochemical and DNA abnormalities;Annals of Neurology;1996-03

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