Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis.
Arwa Z Al-RiyamiAchille IolasconShoaib Al-ZadjaliImmacolata AndolfoSahima Al-MammariFrancesco MannaAbdulHakim Al RawasMay-Jean KingRoberta RussoPublished in: American journal of hematology (2017)