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. |
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| 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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| ISSN: | 23249269 |
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| DOI: | 10.1002/mgg3.1954 |
