Genetic Variations and Neuropathologic Features of Patients with PRKN Mutations-Reference-Cited by-同舟云学术

Genetic Variations and Neuropathologic Features of Patients with PRKN Mutations

Published:2021-02-11 Issue:7 Volume:36 Page:1634-1643
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Seike Naohiko¹²,Yokoseki Akio³,Takeuchi Ryoko¹,Saito Kento⁴,Miyahara Hiroaki¹,Miyashita Akinori⁴,Ikeda Tetsuhiko⁵,Aida Izumi⁵,Nakajima Takashi⁵,Kanazawa Masato³^ORCID,Wakabayashi Masatoshi⁶,Toyoshima Yasuko¹,Takahashi Hitoshi¹,Matsumoto Riki²,Toda Tatsushi⁷,Onodera Osamu³,Ishikawa Atsushi⁸,Ikeuchi Takeshi⁴,Kakita Akiyoshi¹

Affiliation:

1. Department of Pathology Brain Research Institute, Niigata University Niigata Japan

2. Division of Neurology Kobe University Graduate School of Medicine Kobe Japan

3. Department of Neurology Brain Research Institute, Niigata University Niigata Japan

4. Department of Molecular Genetics Brain Research Institute, Niigata University Niigata Japan

5. Department of Neurology NHO Niigata National Hospital Kashiwazaki Japan

6. Department of Neurology Ojiya Sakura Hospital Ojiya Japan

7. Department of Neurology Graduate School of Medicine, The University of Tokyo Tokyo Japan

8. Department of Neurology Brain Disease Center Agano Hospital Agano Japan

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28521

Reference46 articles.

1. Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism

2. Parkin disease: a phenotypic study of a large case series

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5. Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance

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