| 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 |
| Gene_locus related to this paper: human-SERAC1 |
Alagoz M, Kherad N, Turkmen S, Bulut H, Yuksel A (2020)
A novel mutation in the SERAC1 gene correlates with the severe manifestation of the MEGDEL phenotype, as revealed by whole-exome sequencing
Exp Ther Med
19 :3505
Alagoz M, Kherad N, Turkmen S, Bulut H, Yuksel A (2020)
Exp Ther Med
19 :3505