DEAFNESS, AUTOSOMAL DOMINANT 6

Known as: DFNA38, Deafness, Autosomal Dominant 38, DFNA6 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1998-2006
02419982006

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2006
2006
Only three autosomal dominant hearing loss loci (DFNA1, DFNA6/14/38 and DFNA54) have been reported to be associated with… (More)
Is this relevant?
2003
2003
Hereditäre Schwerhörigkeit ist eine extrem heterogene sensorische Erkrankung, wobei die nichtsyndromalen Formen einen Anteil von… (More)
Is this relevant?
2002
2002
AbstractNonsyndromic low-frequency sensorineural hearing loss (LFSNHL) comprises a group (DFNA1, DFNA6, DFNA14, and DFNA38) of… (More)
  • table 1
  • figure 1
  • table 2
  • figure 2
  • figure 3
Is this relevant?
Review
2002
Review
2002
OBJECTIVE To delineate the phenotype and genotype of an autosomal dominant low-frequency sensorineural nonsyndromic hearing… (More)
Is this relevant?
2001
2001
Dominantly inherited progressive hearing loss DFNA38 is caused by heterozygosity for a novel mutation in WFS1, the gene for… (More)
Is this relevant?
2001
2001
The tilted (tlt) mouse carries a recessive mutation causing vestibular dysfunction. The defect in tlt homozygous mice is limited… (More)
  • table 1
  • table 1
  • figure 1
  • table 2
  • figure 2
Is this relevant?
2001
2001
Non-syndromic low frequency sensorineural hearing loss (LFSNHL) affecting only 2000 Hz and below is an unusual type of hearing… (More)
Is this relevant?
1999
1999
Non-syndromic hearing impairment is one of the most heterogeneous hereditary conditions, with more than 40 reported gene… (More)
  • figure 1
  • table 1
  • figure 2
  • figure 4
Is this relevant?
Review
1998
Review
1998
OBJECTIVE To determine if haploinsufficiency for chromosome 4p16.3 in Wolf-Hirschhorn syndrome (WHS) is associated with cochlear… (More)
Is this relevant?