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DFNM1 gene
Known as:
DFNM1
, deafness (recessive, non-syndromic) modifier 1
National Institutes of Health
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1 relation
Broader (1)
Genes
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Modifier variant of METTL13 suppresses human GAB1–associated profound deafness
R. Yousaf
,
Z. Ahmed
,
+7 authors
S. 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…
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Review
2006
Review
2006
Strain background effects and genetic modifiers of hearing in mice
K. Johnson
,
Q. Zheng
,
K. Noben-Trauth
Brain Research
2006
Corpus ID: 20411803
Highly Cited
2000
Highly Cited
2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26
S. Riazuddin
,
C. M. Castelein
,
+9 authors
E. Wilcox
Nature Genetics
2000
Corpus ID: 19347252
More than 50% of severe childhood deafness is genetically determined, approximately 70% of which occurs without other…
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