Retinal and optic nerve abnormalities in neurodegeneration associated with mutations in C19orf12 (MPAN)
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference13 articles.
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2. Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation;Hartig;Am. J. Hum. Genet.,2011
3. New NBIA subtype. Genetic, clinical, pathologic and radiographic features of MPAN;Hogarth;Neurology,2013
4. Genetics and pathophysiology of neurodegeneration with brain Iron accumulation (NBIA);Schneider;Curr. Neuropharmacol.,2013
5. Neuro-ophtalmologic and electroretinographic findings in panthotenate kinase associated neurodegeneration (formerly Hallervorden-Spatz syndrome);Egan;Am J. Ophthalmol.,2005
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