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603629.4
Home
Subject Details
Country
Lebanon
HPO Terms
Hearing impairment
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Sex
Unknown
Parental Consanguinity
Yes
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_005422.4:c.569C>T
2
Deafness, Autosomal Recessive 21
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References
Jalkh et al. 2019
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