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A novel homozygous variation in the PANK2 gene in two Persian siblings with atypical pantothenate kinase associated neurodegeneration
Pantothenate Kinase-associated Neurodegeneration (PKAN) is an autosomal recessive disorder that is caused by variation in pantothenate kinase-2 gene (PANK2) gene on chromosome 20. The common presentation of this disease includes progressive dystonia, Parkinsonism, retinopathy, cognitive impairment,...
Autores principales: | Habibi, Amir Hasan, Razmeh, Saeed, Aryani, Omid, Rohani, Mohammad, Taghavian, Laleh, Alizadeh, Elham, Kokhedan, Karim Moradian, Zaribafian, Maryam |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444562/ https://www.ncbi.nlm.nih.gov/pubmed/30996846 http://dx.doi.org/10.4081/ni.2019.7959 |
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