614067.2

Country

United Arab Emirates

HPO Terms

Global developmental delay; Attention deficit hyperactivity disorder; Intellectual disability; Microcephaly; Spasticity
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Sex

Female

Family History

No

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001128126.1:c.295-3C>A2
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