ArticleMolecular genetics & genomic medicine2022

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.

Lilia Kraoua et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.