Author:
Marshall Randall D.,Collins Abigail,Escolar Maria L.,Jinnah H. A.,Klopstock Thomas,Kruer Michael C.,Videnovic Aleksandar,Robichaux-Viehoever Amy,Burns Colleen,Swett Laura L.,Revicki Dennis A.,Bender Randall H.,Lenderking William R.
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics(clinical),General Medicine
Reference18 articles.
1. Hartig MB, Hortnagel K, Garavaglia B, et al. Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation. Ann Neurol. 2006;59(2):248–56.
2. Hayflick SJ, Westaway SK, Levinson B, et al. Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome. N Engl J Med. 2003;348(1):33–40.
3. Lee JH, Park J, Ryu HS, et al. Clinical heterogeneity of atypical pantothenate kinase-associated neurodegeneration in Koreans. J Mov Disord. 2016;9(1):20–7.
4. National Organization for Rare Disorders. Pantothenate kinase-associated neurodegeneration. 2016; Available at:
https://rarediseases.org/rare-diseases/pantothenate-kinase-associated-neurodegeneration/
. Accessed 27 Nov 2017.
5. Sachin S, Goyal V, Singh S, et al. Clinical spectrum of Hallervorden-Spatz syndrome in India. J Clin Neurosci. 2009;16(2):253–8.
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