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Acta Neurologica Scandinavica|March 12, 2014
Ocular, bulbar, limb, and cardiopulmonary involvement in oculopharyngeal muscular dystrophyN Witting, A Mensah, L Køber, et al.
Acta Neurologica Scandinavica|April 11, 2018
Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndromeN Witting, P Laforêt, N C Voermans, et al.
Acta Neuropathologica|August 30, 2019
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvementS Donkervoort, R Sabouny, P Yun, et al.
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