A novel mutation adjacent to the Bth mouse mutation in the TMC1 gene makes this mouse an excellent model of human deafness at the DFNA36 locus

Benzer Materyaller

• Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at locus DFNA36-DFNB7/11: Four novel TMC1 mutations
  Yazar:: Hilgert, Nele, ve diğerleri
  Baskı/Yayın Bilgisi: (2008)
• A Novel DFNA36 Mutation in TMC1 Orthologous to the Beethoven (Bth) Mouse Associated with Autosomal Dominant Hearing Loss in a Chinese Family
  Yazar:: Zhao, Yali, ve diğerleri
  Baskı/Yayın Bilgisi: (2014)
• Multiple Quantitative Trait Loci Modify Cochlear Hair Cell Degeneration in the Beethoven (Tmc1(Bth)) Mouse Model of Progressive Hearing Loss DFNA36
  Yazar:: Noguchi, Yoshihiro, ve diğerleri
  Baskı/Yayın Bilgisi: (2006)
• miRNA Mutations are Not a Common Cause of Deafness
  Yazar:: Hildebrand, Michael S., ve diğerleri
  Baskı/Yayın Bilgisi: (2010)
• Exonic mutations and exon skipping: lessons learned from DFNA5
  Yazar:: Booth, Kevin T, ve diğerleri
  Baskı/Yayın Bilgisi: (2018)