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A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene.
Tunçer GÖ, Teber S, Albayrak P, Kutluk MG, Deda G. Tunçer GÖ, et al. Among authors: kutluk mg. Turk Pediatri Ars. 2018 Dec 1;53(4):259-262. doi: 10.5152/TurkPediatriArs.2018.4197. eCollection 2018 Dec. Turk Pediatri Ars. 2018. PMID: 30872930 Free PMC article.
16 results