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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 21, 2020 - Issue 7-8
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Brief Report

NEK1 and GRN mutations coexist in a sporadic Chinese Hui descent ALS patient

Kang Zhang1 Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, China National Clinical Research Center for Neurological Diseases, Beijing, ChinaORCID Iconhttps://orcid.org/0000-0002-0170-1314View further author information
ORCID Icon,
Yan Lu2 Department of Intensive Care Unit, The First People’s Hospital of Yinchuan City, Yinchuan, ChinaView further author information
,
Jianhong Chen3 Neuroscience Center, General Hospital of Ningxia Medical University, Key Laboratory of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan, ChinaView further author information
,
Jian Li3 Neuroscience Center, General Hospital of Ningxia Medical University, Key Laboratory of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan, ChinaView further author information
,
Kamal Kishor Yadav3 Neuroscience Center, General Hospital of Ningxia Medical University, Key Laboratory of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan, ChinaView further author information
,
Jiao Yin3 Neuroscience Center, General Hospital of Ningxia Medical University, Key Laboratory of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan, ChinaView further author information
&
Xiao Yang3 Neuroscience Center, General Hospital of Ningxia Medical University, Key Laboratory of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan, ChinaCorrespondence[email protected]
View further author information
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Pages 624-626 | Received 10 Apr 2020, Accepted 03 Jun 2020, Published online: 08 Aug 2020

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