Spectrum of MYO7A Mutations in an Indigenous South African Population Further Elucidates the Nonsyndromic Autosomal Recessive Phenotype of DFNB2 to Include Both Homozygous and Compound Heterozygous Mutations

Míreanna Comhchosúla

• Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss
  le: Wang, Xiao-Hui, et al.
  Foilsithe: (2021)
• Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families
  le: Xu, Pengcheng, et al.
  Foilsithe: (2020)
• A Homozygous Missense Mutation in NEUROD1 Is Associated With Nonsyndromic Autosomal Recessive Retinitis Pigmentosa
  le: Wang, Feng, et al.
  Foilsithe: (2015)
• Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37
  le: Ahmed, Zubair M., et al.
  Foilsithe: (2003)
• Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction
  le: Schraders, Margit, et al.
  Foilsithe: (2010)