Concepedia

Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene

Seyed Bidooki, Margaret Jackson, Margaret A. Johnson, Zofia M. Chrzanowska‐Lightowlers, Robert W. Taylor, Graham Venables, Robert N. Lightowlers, Douglass M. Turnbull, Laurence A. Bindoff

Neuromuscular Disorders · 2004 · 19 citations · 15 references

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References

15

Mfold web server for nucleic acid folding and hybridization prediction

Michael Zuker · Nucleic Acids Research · 2003 · 13.6K citations · Full text

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Sequence and organization of the human mitochondrial genome

Stephen K. Anderson, Alan T. Bankier, B. G. Barrell et al. · Nature · 1981 · 9.7K citations

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A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness

Fiona Reid, G A Vernham, Howard T. Jacobs · Human Mutation · 1994 · 271 citations

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Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNA <sup>Ser(UCN)</sup> gene

Valeria Tiranti, Patrick Chariot, F. Carella et al. · Human Molecular Genetics · 1995 · 209 citations

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A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle.

K. Weber, J Wilson, Louise Taylor et al. · PubMed · 1997 · 201 citations

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