Correlation Engine 2.0
Clear Search sequence regions


  • ichthyosis (1)
  • LCA5 (1)
  • leber amaurosis (1)
  • PNPLA1 (1)
  • Sizes of these terms reflect their relevance to your search.

    No abstract available.

    Citation

    Hui-Juan Zhao, Xin Zeng, Peng-Cheng Lei, Xiao-Dan Jiang, Xue-Min Li, Hui-Min Yan, Du-Yi Guo, Xue-Yan Lu, Wei Jiang. A Chinese family with autosomal recessive congenital ichthyosis and Leber congenital amaurosis due to mutations in PNPLA1 and LCA5. European journal of dermatology : EJD. 2018 Feb 01


    PMID: 29400301

    View Full Text