Clinical and Genetic Features of Multiplex Families with Multiple System Atrophy and Parkinson’s Disease-Reference-Cited by-同舟云学术

Clinical and Genetic Features of Multiplex Families with Multiple System Atrophy and Parkinson’s Disease

Published:2022-09-13 Issue: Volume: Page:
ISSN:1473-4230
Container-title:The Cerebellum
language:en
Short-container-title:Cerebellum

Author:

Matsukawa Takashi,Porto Kristine Joyce L.,Mitsui Jun,Chikada Ayaka,Ishiura Hiroyuki,Takahashi Yuji,Nakamoto Fumiko Kusunoki,Seki Tomonari,Shiio Yasushi,Toda Tatsushi,Tsuji Shoji^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

https://link.springer.com/content/pdf/10.1007/s12311-022-01426-z.pdf

Reference31 articles.

1. Wenning GK, Wagner S, Daniel S, Quinn NP. Multiple system atrophy: sporadic or familial? Lancet. 1993;342:681.

2. Hara K, Momose Y, Tokiguchi S, Shimohata M, Terajima K, Onodera O, et al. Multiplex families with multiple system atrophy. Arch Neurol. 2007;64:545–51.

3. Multiple-System Atrophy Research Collaboration. Mutations in COQ2 in familial and sporadic multiple-system atrophy. N Engl J Med. 2013;369:233–44.

4. Wüllner U, Abele M, Schmitz-Huebsch T, Wilhelm K, Benecke R, Deuschl G, et al. Probable multiple system atrophy in a German family. J Neurol Neurosurg Psychiatry. 2004;75:924–5.

5. Wüllner U, Schmitt I, Kammal M, Kretzschmar HA, Neumann M. Definite multiple system atrophy in a German family. J Neurol Neurosurg Psychiatry. 2009;80:449–50.

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