Novel Compound Heterozygous Mutation in PANK2 in a Patient with an Atypical Form of Pantothenate Kinase Associated Neurodegeneration and His Family
Author:
Publisher
Medknow
Subject
Neurology (clinical),Neurology
Reference11 articles.
1. A novel gene mutation in PANK2 in a patient with an atypical form of pantothenate kinase-associated neurodegeneration;Perez-Gonzalez;Eur J Med Genet,2013
2. Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome;Hayflick;N Engl J Med,2003
3. Clinical and genetic delineation of neurodegeneration with brain iron accumulation;Gregory;J Med Genet,2009
4. Missense PANK2 mutation without “eye of the tiger” sign: MR findings in a large group of patients with pantothenate kinase-associated neurodegeneration (PKAN);Delgado;J Magn Reson Imaging,2012
5. Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration;Zhang;Mov Disord,2005
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