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610220.1
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Subject Details
Country
Morocco
HPO Terms
Profound hearing impairment
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Sex
Male
Family History
Yes
Parental Consanguinity
Yes
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_001042702.5:c.113dup
2
Deafness, Autosomal Recessive 59
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Remarks
Brother of 613862.3.1 (II:2 in the paper)
References
Ebermann et al. 2007
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