DFNM1 gene

Known as: DFNM1, deafness (recessive, non-syndromic) modifier 1 
 
National Institutes of Health

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Genes

Papers overview

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2018
2018
Modifier variant of METTL13 suppresses human GAB1-associated profound deafness.
A modifier variant can abrogate the risk of a monogenic disorder. DFNM1 is a locus on chromosome 1 encoding a dominant suppressor… (More)
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Review
2006
Review
2006
Strain background effects and genetic modifiers of hearing in mice
Genetic modifiers can be detected in mice by looking for strain background differences in inheritance or phenotype of a mutation… (More)
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2000
2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26
More than 50% of severe childhood deafness is genetically determined, approximately 70% of which occurs without other… (More)
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