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Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease
  1. Correspondence to:
 Dr C Toomes, Molecular Medicine Unit, University of Leeds, Clinical Sciences Building, St James’s University Hospital, Leeds LS9 7TF, UK;
 c.toomes{at}leeds.ac.uk
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Citation

Marchbank NJ, Craig JE, Leek JP, et al
Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease

Publication history

  • First published August 1, 2002.
Online issue publication 
April 27, 2016

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