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

समान संसाधन

• Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family
  द्वारा: Gao, Xue, और अन्य
  प्रकाशित: (2015)
• Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1
  द्वारा: Liu, Fei, और अन्य
  प्रकाशित: (2013)
• Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family
  द्वारा: Gao, Xue, और अन्य
  प्रकाशित: (2015)
• Identification of a novel MYO7A mutation in Usher syndrome type 1
  द्वारा: Cheng, Ling, और अन्य
  प्रकाशित: (2017)
• Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing
  द्वारा: Gao, Xue, और अन्य
  प्रकाशित: (2013)