- Tytuł:
- A novel mutation in the SERAC1 gene correlates with the severe manifestation of the MEGDEL phenotype, as revealed by whole-exome sequencing.
- Autorzy:
- Źródło:
- Experimental and therapeutic medicine [Exp Ther Med] 2020 Jun; Vol. 19 (6), pp. 3505-3512. Date of Electronic Publication: 2020 Apr 09.
- Typ publikacji:
- Journal Article
Czasopismo naukowe