A Novel TECTA Mutation in a Dutch DFNA8/12 Family Confirms Genotype–Phenotype Correlation

相似書籍

• Audiological Evaluation of Affected Members from a Dutch DFNA8/12 (TECTA) Family
  由: Plantinga, Rutger F., et al.
  出版: (2006)
• Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction
  由: Schraders, Margit, et al.
  出版: (2010)
• Missense Mutations in POU4F3 Cause Autosomal Dominant Hearing Impairment DFNA15 and Affect Subcellular Localization and DNA Binding
  由: Collin, Rob W.J., et al.
  出版: (2008)
• DFNA8/12 Caused by TECTA Mutations is the Most Identified Subtype of Non-syndromic Autosomal Dominant Hearing Loss
  由: Hildebrand, Michael S., et al.
  出版: (2011)
• Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment
  由: Schraders, Margit, et al.
  出版: (2010)