1 insertion of 2 base pairs
Case#: One patient from Egypt
DiseaseAssertion: MPS1-H
FamilyInfo: Consanguinity present in the family
CasePresentingHPOs: N/A
CaseHPOFreeText: N/A
CaseNotHPOs: N/A
CaseNotHPOFreeText: N/A
CaseEnzymeAssay: N/A
CaseUrineGAGs: N/A
CaseERT: N/A
CaseBMT: N/A
Variant1: c.682insAC in paper but correct nomenclature is c.594_595insAC (p.Leu199ThrfsTer2)
Variant1ClinVarID: N/A
Variant1CAID: CA2586973525
Variant2: c.682insAC in paper but correct nomenclature is c.594_595insAC (p.Leu199ThrfsTer2)
Variant2ClinVarID: N/A
Variant2CAID: CA2586973525
AdditionalVariants: c.346G>A (p.G116R)
ParentalGenotype: N/A
PreviouslyPublished N/A