Different clinical features in siblings with identical mutations of the Parkin gene (PARK2)

Kota Sato; Toru Yamashita; Noriko Hatanaka; Mami Takemoto; Nozomi Hishikawa; Yasuyuki Ohta; Koji Abe

doi:10.1016/j.jns.2016.07.004

Different clinical features in siblings with identical mutations of the Parkin gene (PARK2)

Kota Sato
, Toru Yamashita
, Noriko Hatanaka
, Mami Takemoto
, Nozomi Hishikawa
, Yasuyuki Ohta
, Koji Abe

研究成果 › 査読

本文言語	English
ページ（範囲）	147-149
ページ数	3
ジャーナル	Journal of the neurological sciences
巻	368
DOI	https://doi.org/10.1016/j.jns.2016.07.004
出版ステータス	Published - 9月 15 2016

ASJC Scopus subject areas

神経学
臨床神経学

文献へのアクセス

10.1016/j.jns.2016.07.004

他のファイルとリンク

引用スタイル

@article{b1e7674402ce4dd3b1247480cbfce489,

title = "Different clinical features in siblings with identical mutations of the Parkin gene (PARK2)",

keywords = "Homozygotic exon 3 deletion, PARK2, Parkinson's disease",

author = "Kota Sato and Toru Yamashita and Noriko Hatanaka and Mami Takemoto and Nozomi Hishikawa and Yasuyuki Ohta and Koji Abe",

note = "Funding Information: We are grateful to Dr. Hiroyo Yoshino Ph. D (Research Institute for Diseases of Old Age, Juntendo University School of Medicine, Tokyo, Japan) for her important contributions to the genetic diagnosis of PARK2. This work was partly supported by a Grant-in-Aid for Scientific Research (B) 2529320216 , (C) 24591263 and Challenging Research 24659651 , and by Grants-in-Aid from the Research Committees (Mizusawa H, Nakajima I, Nishizawa M, Sasaki H, and Aoki M) from the Ministry of Health, Labour and Welfare of Japan.",

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T1 - Different clinical features in siblings with identical mutations of the Parkin gene (PARK2)

AU - Sato, Kota

AU - Yamashita, Toru

AU - Hatanaka, Noriko

AU - Takemoto, Mami

AU - Hishikawa, Nozomi

AU - Ohta, Yasuyuki

AU - Abe, Koji

N1 - Funding Information: We are grateful to Dr. Hiroyo Yoshino Ph. D (Research Institute for Diseases of Old Age, Juntendo University School of Medicine, Tokyo, Japan) for her important contributions to the genetic diagnosis of PARK2. This work was partly supported by a Grant-in-Aid for Scientific Research (B) 2529320216 , (C) 24591263 and Challenging Research 24659651 , and by Grants-in-Aid from the Research Committees (Mizusawa H, Nakajima I, Nishizawa M, Sasaki H, and Aoki M) from the Ministry of Health, Labour and Welfare of Japan.

PY - 2016/9/15

Y1 - 2016/9/15

KW - Homozygotic exon 3 deletion

KW - PARK2

KW - Parkinson's disease

UR - https://www.scopus.com/pages/publications/84979071819

UR - https://www.scopus.com/pages/publications/84979071819#tab=citedBy

U2 - 10.1016/j.jns.2016.07.004

DO - 10.1016/j.jns.2016.07.004

M3 - Letter

C2 - 27538620

AN - SCOPUS:84979071819

SN - 0022-510X

VL - 368

SP - 147

EP - 149

JO - Journal of the neurological sciences

JF - Journal of the neurological sciences

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