DEAFNESS, AUTOSOMAL RECESSIVE 63

Known as: DFNB63 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2006-2017
0120062017

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Transmembrane O-methyltransferase (TOMT/LRTOMT) is responsible for non-syndromic deafness DFNB63. However, the specific defects… (More)
Is this relevant?
2013
2013
Hearing loss (HL) is the most frequent sensory defect affecting 1 in 1000 neonates. This can occur due to genetic or… (More)
  • table 1
  • table 2
Is this relevant?
Review
2011
Review
2011
BACKGROUND Hearing loss (HL) is the most frequent sensory birth defect in humans. Autosomal recessive non-syndromic HL (ARNSHL… (More)
  • table 1
  • table 1
  • table 1
  • table 2
  • figure 1
Is this relevant?
2006
2006
Hereditary hearing impairment is a genetically heterogeneous disorder. To date, 49 autosomal recessive nonsyndromic hearing… (More)
  • figure 1
  • figure 2
  • table 1
  • figure 3
  • table 2
Is this relevant?