Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndrome. - Kraoua, Lilia; Jaouadi, Hager; Allouche, Mohamed; Achour, Ahlem; Kaouther, Hakim; Ahmed, Habib Ben; Chaker, Lilia; Maazoul, Faouzi; Ouarda, Fatma; Zaffran, Stéphane; M'rad, Ridha (Molecular Genetics & Genomic Medicine, 2022)