Article info
Online mutation report
Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease
- 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
Citation
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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Copyright 2002 Journal of Medical Genetics