Report for Bulut H

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References (1)

Title : A novel mutation in the SERAC1 gene correlates with the severe manifestation of the MEGDEL phenotype, as revealed by whole-exome sequencing - Alagoz_2020_Exp.Ther.Med_19_3505

Author(s) : Alagoz M , Kherad N , Turkmen S , Bulut H , Yuksel A

Ref : Exp Ther Med , 19 :3505 , 2020

Abstract : Alagoz_2020_Exp.Ther.Med_19_3505

ESTHER : Alagoz_2020_Exp.Ther.Med_19_3505

PubMedSearch : Alagoz_2020_Exp.Ther.Med_19_3505

PubMedID: 32346411

Gene_locus related to this paper: human-SERAC1

Report for Bulut H

General

References (1)

1. A novel mutation in the SERAC1 gene correlates with the severe manifestation of the MEGDEL phenotype, as revealed by whole-exome sequencing