Literature DB >> 28914884

Parkinson disease: CSMD1 gene mutations can lead to familial Parkinson disease.

Mitesh Patel.   

Abstract

Entities:  

Year:  2017        PMID： 28914884     DOI： 10.1038/nrneurol.2017.132

Source DB:  PubMed          Journal:  Nat Rev Neurol        ISSN： 1759-4758            Impact factor:   42.937


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  1 in total

1.  Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson disease.

Authors:  Javier Ruiz-Martínez; Luis J Azcona; Alberto Bergareche; Jose F Martí-Massó; Coro Paisán-Ruiz
Journal:  Neurol Genet       Date:  2017-08-02
  1 in total
  1 in total

1.  A phenomics-based approach for the detection and interpretation of shared genetic influences on 29 biochemical indices in southern Chinese men.

Authors:  Yanling Hu; Aihua Tan; Lei Yu; Chenyang Hou; Haofa Kuang; Qunying Wu; Jinghan Su; Qingniao Zhou; Yuanyuan Zhu; Chenqi Zhang; Wei Wei; Lianfeng Li; Weidong Li; Yuanjie Huang; Hongli Huang; Xing Xie; Tingxi Lu; Haiying Zhang; Xiaobo Yang; Yong Gao; Tianyu Li; Yonghua Jiang; Zengnan Mo
Journal:  BMC Genomics       Date:  2019-12-16       Impact factor: 3.969
  1 in total

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