位置：成果数据库 > 期刊 > 期刊详情页
Two Novel Mutations of Fibrillin-1 GeneCorrelate with Different Phenotypes of Marfan Syndrome in Chi
  • ISSN号：1090-0535
  • 期刊名称：Molecular Vision
  • 时间：2013
  • 页码：751-758
  • 相关项目：抑制mTOR信号通路在老年黄斑变性治疗中的研究
作者： Feng Zhao|Xinyuan Pan|Kanxing Zhao|Chen Zhao|
同期刊论文项目
抑制mTOR信号通路在老年黄斑变性治疗中的研究
期刊论文 12
同项目期刊论文
Targeted Sequencing of 179 Genes Associated withHereditary Retinal Dystrophies and 10 Candidate Gene
一汉族常染色体显性遗传视网膜色素变性家系 视紫红质基因检测分析
A Novel Homozygous BEST1 Mutation Correlateswith Complex Ocular Phenotypes.
SPP2 Mutations Cause AutosomalDominant Retinitis Pigmentosa
Maternal germline mosaicism of kinesin family member 21A(KIF21A) mutation causes complex phenotypes
Novel and Recurrent MYO7A Mutations in UsherSyndrome Type 1 and Type 2
Targeted Next-Generation Sequencing Reveals NovelUSH2A Mutations Associated with Diverse DiseasePhen
PRPF4Mutations Cause Autosomal Dominant Retinitis Pigmentosa.
中国汉族 Leber遗传性视神经病变家系的遗传学检测与分析
慢病毒介导的shRNA靶向干扰mTOR基因表达的稳定小鼠成纤维细胞株的建立