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614035.1
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Subject Details
Country
United Arab Emirates
HPO Terms
Congenital sensorineural hearing impairment
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Sex
Unknown
Subject Variants
Variant Name
Allele Count
Associated Disease
NM_001146079.2:c.278T>G
2
Deafness, Autosomal Recessive 29
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Remarks
Autosomal recessive
References
Elsayed O and Al-Shamsi A. 2022
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CTGA Database
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