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GENETICS

Six SQSTM1 mutations in a Chinese amyotrophic lateral sclerosis cohort

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Pages 378-384 | Received 01 Jul 2014, Accepted 01 Jan 2015, Published online: 24 Feb 2015

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Shinrye Lee, Yu-Mi Jeon, Sun Joo Cha, Seyeon Kim, Younghwi Kwon, Myungjin Jo, You-Na Jang, Seongsoo Lee, Jaekwang Kim, Sang Ryong Kim, Kea Joo Lee, Sung Bae Lee, Kiyoung Kim & Hyung-Jun Kim. (2020) PTK2/FAK regulates UPS impairment via SQSTM1/p62 phosphorylation in TARDBP/TDP-43 proteinopathies. Autophagy 16:8, pages 1396-1412.
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P. A. McCombe, N. R. Wray & R. D. Henderson. (2017) Extra-motor abnormalities in amyotrophic lateral sclerosis: another layer of heterogeneity. Expert Review of Neurotherapeutics 17:6, pages 561-577.
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Danyang Tian, Jiao Li, Lu Tang, Nan Zhang & Dongsheng Fan. (2018) Screening for CCNF Mutations in a Chinese Amyotrophic Lateral Sclerosis Cohort. Frontiers in Aging Neuroscience 10.
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N Shahrizaila, G Sobue, S Kuwabara, S H Kim, Carol Birks, D S Fan, J S Bae, C J Hu, M Gourie-Devi, Y Noto, K Shibuya, K J Goh, R Kaji, CP Tsai, L Cui, P Talman, R D Henderson, S Vucic & M C Kiernan. (2016) Amyotrophic lateral sclerosis and motor neuron syndromes in Asia. Journal of Neurology, Neurosurgery & Psychiatry 87:8, pages 821-830.
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