Article info
Short report
Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity
- Correspondence to: Baziel G M van Engelen Neuromuscular Centre Nijmegen, Institute of Neurology University Medical Centre Nijmegen, PO Box 9101, 6500 HB Nijmegen, the Netherlands; B.vanEngelenneuro.umcn.nl
Citation
Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity
Publication history
- Received August 1, 2003
- Accepted December 23, 2003
- Revised December 5, 2003
- First published September 16, 2004.
Online issue publication
September 16, 2004
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Copyright information
Copyright 2004 Journal of Neurology Neurosurgery and Psychiatry