615330.1

Country

United Arab Emirates

HPO Terms

Global developmental delay; Respiratory failure; Spasticity; Leukoencephalopathy
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001010867.3:c.316A>G2

Remarks

Affected sibling
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