C10ORF2 mutation associated with progressive external ophthalmoplegia and clinically isolated syndrome
- PMID: 28528470
- DOI: 10.1007/s13760-017-0793-8
C10ORF2 mutation associated with progressive external ophthalmoplegia and clinically isolated syndrome
Comment in
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Affection of immune cells by a C10orf2 mutation manifesting as mitochondrial myopathy and transient sensory transverse syndrome.Acta Neurol Belg. 2017 Dec;117(4):969-970. doi: 10.1007/s13760-017-0821-8. Epub 2017 Jul 22. Acta Neurol Belg. 2017. PMID: 28735506 No abstract available.
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