A novel MYH2 mutation in family members presenting with congenital myopathy, ophthalmoplegia and facial weakness

  • Tracey Willis, Carola Hedberg-Oldfors, Zoya Alhaswani, Richa Kulshrestha, Caroline Sewry, Anders Oldfors
  • Deutsche Zeitschrift für Nervenheilkunde, May 2016, Springer Science + Business Media
  • DOI: 10.1007/s00415-016-8154-8

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The following have contributed to this page: Richa Kulshrestha