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

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  • Shahin Asadi

    (Director in the Division of Medical Genetics and Molecular Pathology Research, Iran)

Abstract

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

Suggested Citation

  • Shahin Asadi, 2019. "The Role of Genetic Mutations in Gene PANK2 on Hallervorden-Spatz Syndrome," Biomedical Journal of Scientific & Technical Research, Biomedical Research Network+, LLC, vol. 22(3), pages 16684-16687, November.
    • Handle: RePEc:abf:journl:v:22:y:2019:i:3:p:16684-16687
    DOI: 10.26717/BJSTR.2019.22.003753
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