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A novel OPTN variant causing PSP-CBS-like phenotype in familial amyotrophic lateral sclerosis.
Parkinsonism & Related Disorders ( IF 4.1 ) Pub Date : 2019-11-09 , DOI: 10.1016/j.parkreldis.2019.11.003 Albert Stezin 1 , S P Chaithra 2 , Vikram V Holla 2 , Nitish Kamble 2 , Ravi Yadav 2 , Pramod Kumar Pal 2
中文翻译:
导致家族性肌萎缩性侧索硬化的PSP-CBS样表型的新型OPTN变体。
更新日期:2019-11-01
Parkinsonism & Related Disorders ( IF 4.1 ) Pub Date : 2019-11-09 , DOI: 10.1016/j.parkreldis.2019.11.003 Albert Stezin 1 , S P Chaithra 2 , Vikram V Holla 2 , Nitish Kamble 2 , Ravi Yadav 2 , Pramod Kumar Pal 2
Affiliation
中文翻译:
导致家族性肌萎缩性侧索硬化的PSP-CBS样表型的新型OPTN变体。