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Journal of Genetics

, Volume 85, Issue 1, pp 73–76 | Cite as

A clinical and molecular-genetic analysis of Chinese patients with lattice corneal dystrophy and novel Thr538Pro mutation in theTGFBI (BIGH3) gene

  • Ping Yu
  • Yangshun Gu
  • Yuehong Yang
  • Xiaoyi Yan
  • Liu Chen
  • Zhen Ge
  • Ming Qi
  • Jianmin Si
  • Lei Guo
Research Note

Keywords

lattice corneal dystrophy TGFBI (BIGH3) mutation polymorphism 

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References

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Copyright information

© Indian Academy of Sciences 2006

Authors and Affiliations

  • Ping Yu
    • 1
  • Yangshun Gu
    • 2
  • Yuehong Yang
    • 1
  • Xiaoyi Yan
    • 1
  • Liu Chen
    • 2
  • Zhen Ge
    • 1
  • Ming Qi
    • 1
  • Jianmin Si
    • 3
  • Lei Guo
    • 1
    • 3
  1. 1.Department of Medical GeneticsSchool of MedicineHangzhouChina
  2. 2.Department of Ophthalmology, The First Affiliated HospitalSchool of MedicineHangzhouChina
  3. 3.Research Center for Modeling Human DiseasesZhejiang UniversityHangzhouChina

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