刘奇迹

Administrative Position:副院长

Paper Publications
Whole-exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99.
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  • Affiliation of Author(s):基础医学院
  • Journal:Hum Mutat
  • All the Authors:shaochangshun,lijiangxia,jiangbaichun,Liu
  • First Author:gongyaoqin
  • Indexed by:Unit Twenty Basic Research
  • Document Code:lw-169865
  • Volume:36
  • Issue:1
  • Page Number:98
  • Translation or Not:no
  • Date of Publication:2015-01-01
  • Date of Publication:2015-01-01
Pre One:miR-155 Deficiency Ameliorates Autoimmune Inflammation of Systemic Lupus Erythematosus by Targeting S1pr1 in Faslpr/lpr Mice. Next One:An intronic variant associated with systemic lupus erythematosus changes the binding affinity of Yinyang1 to downregulate WDFY4.
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