Familial idiopathic basal ganglia calcification: Histopathologic features of an autopsied patient with anSLC20A2mutation-Reference-Cited by-同舟云学术

Familial idiopathic basal ganglia calcification: Histopathologic features of an autopsied patient with anSLC20A2mutation

Published:2015-12-04 Issue:4 Volume:36 Page:365-371
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Kimura Tadashi¹,Miura Takeshi²³,Aoki Kenju³,Saito Shoji⁴,Hondo Hiroaki⁴,Konno Takuya²,Uchiyama Akio⁵,Ikeuchi Takeshi⁶,Takahashi Hitoshi¹,Kakita Akiyoshi¹

Affiliation:

1. Departments of Pathology, Brain Research Institute; University of Niigata; Niigata Japan

2. Departments of Neurology, Brain Research Institute; University of Niigata; Niigata Japan

3. Departments of Neurology; Toyama Prefectural Central Hospital; Toyama Japan

4. Departments of Neurosurgery; Toyama Prefectural Central Hospital; Toyama Japan

5. Departments of Pathology; Toyama Prefectural Central Hospital; Toyama Japan

6. Departments of Molecular Genetics, Brain Research Institute; University of Niigata; Niigata Japan

Publisher

Wiley

Subject

Neurology (clinical),General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12280/fullpdf

Reference36 articles.

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3. Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease);Geschwind;Am J Hum Genet,1999

4. 2q37 as a susceptibility locus for idiopathic basal ganglia calcification (IBGC) in a large South Tyrolean family;Volpato;J Mol Neurosci,2009

5. Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification;Dai;Am J Med Genet B Neurospychiatr Genet,2010

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