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 - Aix-Marseille Université Access content directly
Journal Articles MOLECULAR GENETICS & GENOMIC MEDICINE Year : 2022

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

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Genetics

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hal-03780229 , version 1 (19-09-2022)

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Lilia Kraoua, Hager Jaouadi, Mohamed Allouche, Ahlem Achour, Hakim Kaouther, et al.. 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. MOLECULAR GENETICS & GENOMIC MEDICINE, 2022, 10 (7), ⟨10.1002/mgg3.1954⟩. ⟨hal-03780229⟩
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