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. 1998 Dec;63(6):1594–1597. doi: 10.1086/302169
Getting to the nucleus of mitochondrial disorders: identification of respiratory chain-enzyme genes causing Leigh syndrome.
H H Dahl
1
H H Dahl
1The Murdoch Institute, Royal Children's Hospital, Melbourne, Australia. dahl@cryptic.rch.unimelb.edu.au
Find articles by H H Dahl
1The Murdoch Institute, Royal Children's Hospital, Melbourne, Australia. dahl@cryptic.rch.unimelb.edu.au
PMCID: PMC1377630 PMID: 9837811
See the article "The first nuclear-encoded complex I mutation in a patient with Leigh syndrome." on page 1598.
See the article "Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency." on page 1609.