A gel electrophoresis method for detection of mitochondrial DNA mutation (3243 tRNALeu (UUR)) applied to a Norwegian family with diabetes mellitus and hearing loss-Reference-Cited by-同舟云学术

A gel electrophoresis method for detection of mitochondrial DNA mutation (3243 tRNALeu (UUR)) applied to a Norwegian family with diabetes mellitus and hearing loss

Published:2004-04 Issue:2 Volume:64 Page:86-92
ISSN:0036-5513
Container-title:Scandinavian Journal of Clinical and Laboratory Investigation
language:en
Short-container-title:Scandinavian Journal of Clinical and Laboratory Investigation

Author:

Akbari M.,Skjelbred C.,Følling I.,Sagen J.,Krokan H. E.

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.1080/00365510410004209

Reference12 articles.

1. Mitochondrial genetics and disease

2. Mitochondrial DNA analysis: polymorphisms and pathogenicity

3. Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

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