618050.1

Country

United Arab Emirates

HPO Terms

Global developmental delay; Attention deficit hyperactivity disorder
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Sex

Male

Family History

No

Parental Consanguinity

No

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001284333.1:c.1850C>T1

Remarks

de novo mutation
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