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611092.1
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Subject Details
Country
Saudi Arabia
HPO Terms
Global developmental delay; Seizure; Microcephaly; Intellectual disability, severe
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Sex
Female
Family History
Yes
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_021956.5:c.2179C>T
2
Intellectual Developmental Disorder, Autosomal Recessive 6
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References
Monies et al. 2017
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