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Frequency of rare mitochondrial DNA mutations in patients with suspected Leber’s hereditary optic neuropathy
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  1. Correspondence to:
 Dr P F Chinnery, Neurology, The Medical School, Framlington Place, Newcastle upon Tyne NE2 4HH, UK; 
 P.F.Chinnery{at}ncl.ac.uk
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Citation

Taylor RW, Jobling MS, Turnbull DM, et al
Frequency of rare mitochondrial DNA mutations in patients with suspected Leber’s hereditary optic neuropathy

Publication history

  • First published July 1, 2003.
Online issue publication 
July 01, 2003

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