A novel MYH2 mutation in family members presenting with congenital myopathy, ophthalmoplegia and facial weakness
Crossref DOI link: https://doi.org/10.1007/s00415-016-8154-8
Published Online: 2016-05-13
Published Print: 2016-07
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Willis, Tracey
Hedberg-Oldfors, Carola
Alhaswani, Zoya
Kulshrestha, Richa
Sewry, Caroline
Oldfors, Anders
Funding for this research was provided by:
The Swedish Research Council (07122)
Text and Data Mining valid from 2016-05-13