Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variants

समान संसाधन

• AON-based degradation of c.151C>T mutant COCH transcripts associated with dominantly inherited hearing impairment DFNA9
  द्वारा: Erik de Vrieze, और अन्य
  प्रकाशित: (2021-06-01)
• Unraveling haplotype errors in the DFNA33 locus
  द्वारा: Barbara Vona, और अन्य
  प्रकाशित: (2023-08-01)
• DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the Literature
  द्वारा: Ugo Sorrentino, और अन्य
  प्रकाशित: (2021-10-01)
• Constitutive activation of DIA1 (DIAPH1) via C‐terminal truncation causes human sensorineural hearing loss
  द्वारा: Takehiko Ueyama, और अन्य
  प्रकाशित: (2016-10-01)
• Correlations Between Vestibular Function and Imaging of the Semicircular Canals in DFNA9 Patients
  द्वारा: Berina Ihtijarevic, और अन्य
  प्रकाशित: (2020-01-01)