Aortic disease and cardiomyopathy in patients with a novel DNMT3A gene variant causing Tatton-Brown–Rahman syndrome.

Autor: Zebrauskiene, Dovile1 (AUTHOR) dovile.zebrauskiene@mf.stud.vu.lt, Sadauskiene, Egle2 (AUTHOR), Dapkunas, Justas3 (AUTHOR), Kairys, Visvaldas3 (AUTHOR), Balciunas, Joris4 (AUTHOR), Konovalovas, Aleksandras5 (AUTHOR), Masiuliene, Ruta6 (AUTHOR), Petraityte, Gunda1 (AUTHOR), Valeviciene, Nomeda7 (AUTHOR), Mataciunas, Mindaugas7 (AUTHOR), Barysiene, Jurate2 (AUTHOR), Mikstiene, Violeta1 (AUTHOR), Tomkuviene, Migle4 (AUTHOR) migle.tomkuviene@bti.vu.lt, Preiksaitiene, Egle1 (AUTHOR)
Zdroj: Clinical Epigenetics. 6/6/2024, Vol. 16 Issue 1, p1-15. 15p.
Databáze: Academic Search Ultimate
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