Distinctive features of degenerating P urkinje cells in spinocerebellar ataxia type 31-Reference-Cited by-同舟云学术

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Distinctive features of degenerating P urkinje cells in spinocerebellar ataxia type 31

Published:2013-12-17 Issue:3 Volume:34 Page:261-267
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Yoshida Kunihiro¹,Asakawa Mika²,Suzuki‐Kouyama Emi²,Tabata Kenichi³,Shintaku Masayuki⁴,Ikeda Shu‐ichi⁵,Oyanagi Kiyomitsu²

Affiliation:

1. Division of Neurogenetics Department of Brain Disease Research Shinshu University School of Medicine Matsumoto Japan

2. Division of Neuropathology Department of Brain Disease Research Shinshu University School of Medicine Matsumoto Japan

3. Department of Neurology Saku Central Hospital Saku Japan

4. Department of Pathology Osaka Red Cross Hospital Osaka Japan

5. Department of Medicine (Neurology and Rheumatology) Shinshu University School of Medicine Matsumoto Japan

Publisher

Wiley

Subject

Clinical Neurology,General Medicine,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/neup.12090

Reference14 articles.

1. Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians

2. SCA in Korea and its regional distribution: A multicenter analysis

3. Spinocerebellar ataxia type 31 exists in Northeast China

4. Spinocerebellar Ataxia Type 31 Is Associated with “Inserted” Penta-Nucleotide Repeats Containing (TGGAA)n

5. Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan

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