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• W1835703087 abstract "Movement DisordersVolume 29, Issue 3 p. 307-307 Hot Topics A new gene for Fahr's syndrome—PDGF-B Amit Batla MD, Amit Batla MD Sobell Department of Motor Neuroscience and Movement disorders, UCL Institute of Neurology, London, United KingdomSearch for more papers by this authorKailash P. Bhatia MD, FRCP, Kailash P. Bhatia MD, FRCP Sobell Department of Motor Neuroscience and Movement disorders, UCL Institute of Neurology, London, United KingdomSearch for more papers by this author Amit Batla MD, Amit Batla MD Sobell Department of Motor Neuroscience and Movement disorders, UCL Institute of Neurology, London, United KingdomSearch for more papers by this authorKailash P. Bhatia MD, FRCP, Kailash P. Bhatia MD, FRCP Sobell Department of Motor Neuroscience and Movement disorders, UCL Institute of Neurology, London, United KingdomSearch for more papers by this author First published: 03 January 2014 https://doi.org/10.1002/mds.25788Citations: 3 Relevant conflicts of interest/financial disclosures: Nothing to report. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL No abstract is available for this article. References 1Delacour A. Ossification des capillaires du cerveau. Annalesde Medecine et Psychologie 1850; 2: 458- 461. 2 Fahr. Idiopathische Verkalkung derflirngefasse. Zentralblatt Allgemeine Pathologie 1930; 50: 129- 133. 3Boller F, Boller M, Gilbert J. Familial idiopathic cerebral calcifications. J Neurol Neurosurg Psychiatry 1977; 40: 280- 285. 4Geschwind DH, Loginov M, Stern JM. Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). Am J Hum Genet 1999; 65: 764- 772. 5Volpato CB, De Grandi A, Buffone E, et al. 2q37 as a susceptibility locus for idiopathic basal ganglia calcification (IBGC) in a large South Tyrolean family. J Mol Neurosci 2009; 39: 346- 353. 6Dai X, Gao Y, Xu Z, et al. Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification. Am J Med Genet B Neuropsychiatr Genet 2010; 153B: 1305- 1310. 7Nicolas G, Pottier C, Maltete D, et al. Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification. Neurology 2013; 80: 181- 187. 8Chen W-J, Yao X-P, Zhang Q-J, et al. Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification. Gene 2013; 529: 159- 162. 9Keller A, Westenberger A, Sobrido MJ, et al. Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice. Nat Genet 2013; 45: 1077- 1082. 10Hsu SC, Sears RL, Lemos RR, et al. Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification. Neurogenetics 2013; 14: 11- 22. Citing Literature Volume29, Issue3March 2014Pages 307-307 ReferencesRelatedInformation" @default.
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• W1835703087 title "A new gene for Fahr's syndrome-<i>PDGF-B</i>" @default.
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