Homozygous deletion in CDH3 and hypotrichosis with juvenile macular dystrophy.

समान संसाधन

• Characterization of CDH3-related congenital hypotrichosis with juvenile macular dystrophy
  द्वारा: Hull, S, और अन्य
  प्रकाशित: (2016)
• Hypotrichosis and juvenile macular dystrophy caused by CDH3 mutation: A candidate disease for retinal gene therapy
  द्वारा: Singh, M, और अन्य
  प्रकाशित: (2016)
• The first Japanese family of CDH3‐related hypotrichosis with juvenile macular dystrophy
  द्वारा: Takaaki Hayashi, और अन्य
  प्रकाशित: (2021-06-01)
• CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
  द्वारा: Omer Karti, और अन्य
  प्रकाशित: (2017-09-01)
• Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
  द्वारा: Yunqing Ren, और अन्य
  प्रकाशित: (2022-06-01)