A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations

Transl Neurodegener. 2021 Oct 28;10(1):42. doi: 10.1186/s40035-021-00266-x.

Lu Tang^#^{1

2}, Johannes Dorst^#^{3

4}, Lu Chen^{1

2}, Xiaolu Liu^{1

2}, Yan Ma^{1

2}, Kornelia Günther³, Sebastian Michels³, Kathrin Müller³, Axel Freischmidt³, Jochen H Weishaupt³, Dongsheng Fan^{5

6}, Albert C Ludolph^{7

8}

¹ Department of Neurology, Peking University Third Hospital, Beijing, 100191, China.
² Beijing Key Laboratory of Biomarker and Translational Research in Neurodegenerative Diseases, Peking University Third Hospital, Beijing, 100191, China.
³ Department of Neurology, Ulm University, 89081, Ulm, Germany.
⁴ German Center for Neurodegenerative Diseases (DZNE), Ulm Site, 89081, Ulm, Germany.
⁵ Department of Neurology, Peking University Third Hospital, Beijing, 100191, China. dsfan2010@aliyun.com.
⁶ Beijing Key Laboratory of Biomarker and Translational Research in Neurodegenerative Diseases, Peking University Third Hospital, Beijing, 100191, China. dsfan2010@aliyun.com.
⁷ Department of Neurology, Ulm University, 89081, Ulm, Germany. Albert.Ludolph@rku.de.
⁸ German Center for Neurodegenerative Diseases (DZNE), Ulm Site, 89081, Ulm, Germany. Albert.Ludolph@rku.de.

^# Contributed equally.

No abstract available

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