Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia (Q24297970)

From Wikidata
Jump to navigation Jump to search
scientific article
edit
Language Label Description Also known as
English
Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia
scientific article

    Statements

    Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia (English)
    0 references
    Wan-Jin Chen
    0 references
    Yu Lin
    0 references
    Zhi-Qi Xiong
    0 references
    Wei Wei
    0 references
    Wang Ni
    0 references
    Guo-He Tan
    0 references
    Shun-Ling Guo
    0 references
    Jin He
    0 references
    Ya-Fang Chen
    0 references
    Qi-Jie Zhang
    0 references
    Hong-Fu Li
    0 references
    Yi Lin
    0 references
    Shen-Xing Murong
    0 references
    Jianfeng Xu
    0 references
    Ning Wang
    0 references
    Zhi-Ying Wu
    0 references
    December 2011
    0 references
    43
    0 references
    12
    0 references
    1252-5
    0 references

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit