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DEAFNESS, AUTOSOMAL RECESSIVE 26

Known as: DFNB26 
National Institutes of Health

Papers overview

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2018
2018
  • R. Yousaf, Zubair M. Ahmed, +7 authors Saima Riazuddin
  • The Journal of clinical investigation
  • 2018
  • Corpus ID: 4626954
A modifier variant can abrogate the risk of a monogenic disorder. DFNM1 is a locus on chromosome 1 encoding a dominant suppressor… Expand
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Highly Cited
2000
Highly Cited
2000
More than 50% of severe childhood deafness is genetically determined, approximately 70% of which occurs without other… Expand
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