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601071.4
Home
Subject Details
Country
United Arab Emirates
HPO Terms
Hearing impairment
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Sex
Unknown
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_194248.3:c.5159C>T
1
Deafness, Autosomal Recessive 9
NM_194248.3:c.2374C>T
1
Deafness, Autosomal Recessive 9
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References
Tlili et al. 2024
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