A Novel Locus (DFNA24) for Prelingual Nonprogressive Autosomal Dominant Nonsyndromic Hearing Loss Maps to 4q35-qter in a Large Swiss German Kindred

समान संसाधन

• A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred.
  द्वारा: Salam, A A, और अन्य
  प्रकाशित: (2000)
• Phenotypic Characterization of DFNA24 : Prelingual Progressive Sensorineural Hearing Impairment
  द्वारा: Santos, Regie Lyn P., और अन्य
  प्रकाशित: (2006)
• A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval
  द्वारा: DeWan, AT, और अन्य
  प्रकाशित: (2003)
• Human Nonsyndromic Hereditary Deafness DFNA17 Is Due to a Mutation in Nonmuscle Myosin MYH9
  द्वारा: Lalwani, Anil K., और अन्य
  प्रकाशित: (2000)
• Identification of a Novel TECTA Mutation in a Chinese DFNA8/12 Family with Prelingual Progressive Sensorineural Hearing Impairment
  द्वारा: Li, Zhengyue, और अन्य
  प्रकाशित: (2013)