Literature DB >> 32892228

Reply: Segregation of ATP10B variants in families with autosomal recessive Parkinsonism.

Stefanie Smolders1, Christine Van Broeckhoven2.   

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Year:  2020        PMID： 32892228     DOI： 10.1007/s00401-020-02220-z

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN： 0001-6322            Impact factor:   17.088


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  2 in total

1.  ATP10B variants in Parkinson's disease: a large cohort study in Chinese mainland population.

Authors:  Yuwen Zhao; Hongxu Pan; Yige Wang; Qian Zeng; Zhenghuan Fang; Runcheng He; Kun Xu; Xiaoxia Zhou; Xun Zhou; Zhou Zhou; Yanghong Li; Penghui Deng; Yinghui Xu; Qian Xu; Qiying Sun; Bin Li; Guihu Zhao; Lifang Lei; Hainan Zhang; Chunyu Wang; Jieqiong Tan; Xinxiang Yan; Lu Shen; Hong Jiang; Jinchen Li; Jifeng Guo; Beisha Tang; Zhenhua Liu
Journal:  Acta Neuropathol       Date:  2021-02-18       Impact factor: 17.088

2.  Reply: ATP10B variants in Parkinson's disease-a large cohort study in Chinese mainland population.

Authors:  Stefanie Smolders; Christine Van Broeckhoven
Journal:  Acta Neuropathol       Date:  2021-02-18       Impact factor: 17.088
  2 in total

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