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Paper Report for: Alagoz_2020_Exp.Ther.Med_19_3505

Reference

Title: A novel mutation in the SERAC1 gene correlates with the severe manifestation of the MEGDEL phenotype, as revealed by whole-exome sequencing
Alagoz M, Kherad N, Turkmen S, Bulut H, Yuksel A
Ref: Exp Ther Med, 19:3505, 2020 : PubMed

        



Related information

Gene_Locus| human-SERAC1
Mutation | G339R_human-SERAC1,



Citations formats

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: 3505-3512

Alagoz M, Kherad N, Turkmen S, Bulut H, Yuksel A (2020)
Exp Ther Med 19: 3505-3512



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