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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 |