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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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Title: 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.
Authors: Kraoua, Lilia1,2 (AUTHOR), Jaouadi, Hager3 (AUTHOR), Allouche, Mohamed4 (AUTHOR), Achour, Ahlem1,2 (AUTHOR), Kaouther, Hakim5 (AUTHOR), Ahmed, Habib Ben6 (AUTHOR), Chaker, Lilia7 (AUTHOR), Maazoul, Faouzi1 (AUTHOR), Ouarda, Fatma5 (AUTHOR), Zaffran, Stéphane3 (AUTHOR) stephane.zaffran@univ‐amu.fr, M'rad, Ridha1,2 (AUTHOR)
Source: Molecular Genetics & Genomic Medicine. Jul2022, Vol. 10 Issue 7, p1-8. 8p.
Database: Academic Search Ultimate
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  Data: 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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  Data: <searchLink fieldCode="JN" term="%22Molecular+Genetics+%26+Genomic+Medicine%22">Molecular Genetics & Genomic Medicine</searchLink>. Jul2022, Vol. 10 Issue 7, p1-8. 8p.
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        Value: 10.1002/mgg3.1954
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        Text: English
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      – TitleFull: 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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            – D: 01
              M: 07
              Text: Jul2022
              Type: published
              Y: 2022
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