614701.1

Country

United Arab Emirates

HPO Terms

Microcephaly; Failure to thrive; Global developmental delay; Hypertonia
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Sex

Female

Family History

No

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_006265.2:c.1432C>T1

Remarks

de novo mutation
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