Author:
Deutschländer Angela,Konno Takuya,Ross Owen A.
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference14 articles.
1. The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN;Olgiati;Park. Relat. Disord.,2017
2. Evolution and novel radiological changes of neurodegeneration associated with mutations in C19orf12;Skowronska;Park. Relat. Disord.,2017
3. Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation;Hartig;Am. J. Hum. Genet.,2011
4. New NBIA subtype: genetic, clinical, pathologic, and radiographic features of MPAN;Hogarth;Neurology,2013
5. Review: insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories;Arber;Neuropathol. Appl. Neurobiol.,2016
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