Abstract
Mitochondrial cytochrome b mutations have been reported to have a homogenous phenotype of pure exercise intolerance. We describe a novel mutation in the cytochrome b gene of mitochondrial DNA (A15579G) associated with a selective decrease of muscle complex III activity in a patient who, besides severe exercise intolerance, also has multisystem manifestations (deafness, mental retardation, retinitis pigmentosa, cataract, growth retardation, epilepsy). The point mutation is heteroplasmic in muscle (88%) and leukocytes (15%), and changes a highly conserved tyrosine to cysteine at amino acid position 278.
Originalsprog | Engelsk |
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Tidsskrift | Annals of Neurology |
Vol/bind | 50 |
Udgave nummer | 4 |
Sider (fra-til) | 540-3 |
Antal sider | 4 |
ISSN | 0364-5134 |
DOI | |
Status | Udgivet - okt. 2001 |