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615905.1
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Subject Details
Country
Saudi Arabia
HPO Terms
Microcephaly; Seizure; Hypotonia; Severe global developmental delay
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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_177550.5:c.1227dup
2
Developmental and Epileptic Encephalopathy 25 with Amelogenesis Imperfecta
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References
Monies et al. 2017
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