Optic Atrophy in a Patient With Atypical Pantothenate Kinase-Associated Neurodegeneration
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Clinical Neurology,Ophthalmology
Reference17 articles.
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1. Case report: Novel compound heterozygous variants in the PANK2 gene in a Chinese patient diagnosed with ASD and ADHD;Frontiers in Neurology;2023-04-17
2. Psychiatric symptoms in an adolescent reveal a novel compound heterozygous mutation of the PANK2 gene in the atypical PKAN syndrome;Psychiatric Genetics;2021-04-12
3. Atypical pantothenate kinase-associated neurodegeneration with PANK2 mutations : clinical description and a review of the literature;Neurocase;2020-04-20
4. Ophthalmological changes in hereditary spastic paraplegia and other genetic diseases with spastic paraplegia;Journal of the Neurological Sciences;2020-02
5. Novel compound heterozygous PANK2 gene mutations in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration;International Journal of Neuroscience;2018-08-15
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