Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family

مواد مشابهة

• Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family
  بواسطة: Gao, Xue, وآخرون
  منشور في: (2014)
• Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1
  بواسطة: Liu, Fei, وآخرون
  منشور في: (2013)
• Identification of a novel MYO7A mutation in Usher syndrome type 1
  بواسطة: Cheng, Ling, وآخرون
  منشور في: (2017)
• Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family
  بواسطة: Gao, Xue, وآخرون
  منشور في: (2015)
• Phenotype of Usher syndrome type II assosiated with compound missense mutations of c.721 C>T and c.1969 C>T in MYO7A in a Chinese Usher syndrome family
  بواسطة: Zhai, Wei, وآخرون
  منشور في: (2015)