Phenotype variability in 130 adult patients with respiratory chain disorders-Reference-Cited by-同舟云学术

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Phenotype variability in 130 adult patients with respiratory chain disorders

Published:2001-10 Issue:5 Volume:24 Page:560-576
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Finsterer J.¹²,Jarius C.³,Eichberger H.⁴,Jaksch M.⁵

Affiliation:

1. ; Neurological Department; Neurological Hospital Rosenhügel; Vienna Austria

2. Ludwig Boltzmann Institute for Epilepsy and Neuromuscular Disorders; Vienna Austria

3. ; Institute of Clinical Neurology; University of Vienna; Vienna Austria

4. ; Neuromuscular Department, Anatomical Institute; University of Vienna; Vienna Austria

5. Institute of Clinical Chemistry; Molecular Diagnostics and Mitochondrial Genetics; Munich Germany

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1012415810881/fullpdf

Reference36 articles.

1. Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA;Andreu;N Engl J Med,1999

2. Clinical features, investigation, and management of patients with defects of mitochondrial DNA;Chinnery;J Neurol Neurosurg Psychiatry,1997

3. Molecular pathology of MELAS and MERRF. The relation between mutation and clinical phenotypes;Chinnery;Brain,1997

4. Mitochondrial encephalomyopathies: back to mendelian genetics;DiMauro;Ann Neurol,1999

5. Functional involvement of central nervous system in mitochondrial disorders;DiLazzaro;Electroencephalogr Clin Neurophysiol,1997

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