Mitochondrial Disorders. A Diagnostic Challenge in Clinical Chemistry-Reference-Cited by-同舟云学术

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Mitochondrial Disorders. A Diagnostic Challenge in Clinical Chemistry

Published:1999-01-15 Issue:9 Volume:37 Page:
ISSN:1434-6621
Container-title:Clinical Chemistry and Laboratory Medicine
language:
Short-container-title:

Author:

Bauer Matthias F.,Gempel Klaus,Hofmann Sabine,Jaksch Michaela,Philbrook Christine,Gerbitz Klaus-Dieter

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Link

https://www.degruyter.com/document/doi/10.1515/CCLM.1999.129/pdf

Reference202 articles.

1. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

2. Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy

3. MITOMAP: a human mitochondrial genome database--1998 update

4. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

5. The First Nuclear-Encoded Complex I Mutation in a Patient with Leigh Syndrome

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