Diagnosing MERRF requires clinical and genetic evidence
Open Access
- 4 September 2019
- journal article
- letter
- Published by Termedia Sp. z.o.o. in Polish Journal of Pathology
- Vol. 70 (2) , 144-145
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
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- Mitochondrial multiorgan disorder syndrome score generated from definite mitochondrial disordersNeuropsychiatric Disease and Treatment, 2017
- Expanded phenotypic spectrum of the m.8344A>G “MERRF” mutation: data from the German mitoNET registryJournal of Neurology, 2016
- When should MERRF (myoclonus epilepsy associated with ragged-red fibers) be the diagnosis?Arquivos de Neuro-Psiquiatria, 2014