Dalili S

References (1)

Title : Reporting a Novel Disease Causing Variant in PGAP3 Associated With Hyperphosphatasia and Intellectual Disability: A Case Report and Comprehensive Literature Review - Salmaninejad_2026_Mol.Genet.Genomic.Med_14_e70206

Author(s) : Salmaninejad A , Seyedtaghia MR , Bereshneh AH , Azizi N , Bayat R , Esnaashari S , Aminzadeh V , Koohmanaee S , Savad S , Mojarrad M , Dalili S

Ref : Mol Genet Genomic Med , 14 :e70206 , 2026

Abstract :

PubMedSearch : Salmaninejad_2026_Mol.Genet.Genomic.Med_14_e70206

PubMedID: 41866703

Dalili S

References (1)

1. Reporting a Novel Disease Causing Variant in PGAP3 Associated With Hyperphosphatasia and Intellectual Disability: A Case Report and Comprehensive Literature Review - Salmaninejad_2026_Mol.Genet.Genomic.Med_14_e70206