Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

DEAFNESS, AUTOSOMAL RECESSIVE 63

Known as: DFNB63 
 
National Institutes of Health

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… Expand
Is this relevant?
2014
2014
1. Department of Genetic, Faculty of Science, ShahidChamran University of Ahwaz, Ahwaz, Iran. 2. Cellular and Molecular Biology… Expand
  • 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… Expand
  • table 1
  • table 1
  • table 1
  • table 2
  • figure 1
Is this relevant?
2007
2007
Hereditary hearing impairment is the most genetically heterogeneous trait known in humans. So far, 50 published autosomal… Expand
Is this relevant?
2006
2006
A genome wide linkage analysis of nonsyndromic deafness segregating in a consanguineous Pakistani family (PKDF537) was used to… Expand
  • figure 1
  • table 1
  • figure 2
Is this relevant?
2006
2006
Hereditary hearing impairment is a genetically heterogeneous disorder. To date, 49 autosomal recessive nonsyndromic hearing… Expand
  • figure 1
  • figure 2
  • table 1
  • figure 3
  • table 2
Is this relevant?