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615761.1
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Subject Details
Country
United Arab Emirates
HPO Terms
Global developmental delay; Hypoglycemia; Polydactyly
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Sex
Female
Family History
No
Parental Consanguinity
No
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_001080517.2:c.2347-7A>G
1
Mental Retardation, Autosomal Dominant 23
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Remarks
de novo mutation
References
Saleh et al. 2021
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