Audiological Evaluation of Affected Members from a Dutch DFNA8/12 (TECTA) Family

Samankaltaisia teoksia

• A Novel TECTA Mutation in a Dutch DFNA8/12 Family Confirms Genotype–Phenotype Correlation
  Tekijä: Plantinga, Rutger F., et al.
  Julkaistu: (2006)
• DFNA8/12 Caused by TECTA Mutations is the Most Identified Subtype of Non-syndromic Autosomal Dominant Hearing Loss
  Tekijä: Hildebrand, Michael S., et al.
  Julkaistu: (2011)
• Identification of a Novel TECTA Mutation in a Chinese DFNA8/12 Family with Prelingual Progressive Sensorineural Hearing Impairment
  Tekijä: Li, Zhengyue, et al.
  Julkaistu: (2013)
• Missense Mutations in POU4F3 Cause Autosomal Dominant Hearing Impairment DFNA15 and Affect Subcellular Localization and DNA Binding
  Tekijä: Collin, Rob W.J., et al.
  Julkaistu: (2008)
• Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction
  Tekijä: Schraders, Margit, et al.
  Julkaistu: (2010)