The Role of Genetic Mutations in Gene PANK2 on Hallervorden-Spatz Syndrome

Shahin Asadi
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Shahin Asadi: Director in the Division of Medical Genetics and Molecular Pathology Research, Iran

Biomedical Journal of Scientific & Technical Research, 2019, vol. 22, issue 3, 16684-16687

Abstract: Pantothenate kinase-associated neurodegeneration (PKAN), formerly called Hallervorden-Spatz syndrome, is a rare, inherited neurological movement disorder characterized by the progressive degeneration...

Keywords: Journal on Medical Science; Open Access Medical Journal; Free Medical Journal; American Medical Journal; Top Medical Open Access Journal; Medical and Medicinal Journal; Open Access Clinical and Medical Journal; Pathology Open Access Journal; Pathology Journal; Journals on Pathology; Neurodegenerative Disorder; Hallervorden-Spatz Syndrome; Neurological Movement; Etiology Speech Problems; Visual Loss; Dementia; Psychiatric Symptoms; Pathology; Co-Enzyme; Carbohydrates; Health Care; Dystonia (search for similar items in EconPapers)
Date: 2019
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Persistent link: https://EconPapers.repec.org/RePEc:abf:journl:v:22:y:2019:i:3:p:16684-16687

DOI: 10.26717/BJSTR.2019.22.003753

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