Identification of a novel mutation in the ABCA4 gene in a Chinese family with retinitis pigmentosa using exome sequencing

مواد مشابهة

• Heterozygous RHO p.R135W missense mutation in a large Han-Chinese family with retinitis pigmentosa and different refractive errors
  بواسطة: Wu, Yuan, وآخرون
  منشور في: (2019)
• Identification of novel pathogenic ABCA4 variants in a Han Chinese family with Stargardt disease
  بواسطة: Xiang, Qin, وآخرون
  منشور في: (2019)
• Identification of a Heterozygous Mutation in the TGFBI Gene in a Hui-Chinese Family with Corneal Dystrophy
  بواسطة: Xiang, Qin, وآخرون
  منشور في: (2019)
• Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing.
  بواسطة: Hao Deng, وآخرون
  منشور في: (2016-01-01)
• Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing
  بواسطة: Deng, Hao, وآخرون
  منشور في: (2016)