Oculopharyngodistal myopathy is a distinct entity: Clinical and genetic features of 47 patients
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[1] K. Bushby,et al. Oculopharyngodistal myopathy is a distinct entity , 2011, Neurology.
[2] B. V. van Engelen,et al. Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity , 2004, Journal of Neurology, Neurosurgery & Psychiatry.
[3] I. Nonaka,et al. Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy , 2002, Neurology.
[4] I. Nonaka,et al. Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy , 2001, Neuromuscular Disorders.
[5] M. Uchino,et al. Autosomal recessive oculopharyngodistal myopathy in light of distal myopathy with rimmed vacuoles and oculopharyngeal muscular dystrophy , 1998, Neuromuscular Disorders.
[6] E. Satoyoshi,et al. Oculopharyngodistal myopathy. , 1977, Archives of neurology.