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Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy.

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Title: Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy.
Authors: Manivannan, Sathiya N.1,2 (AUTHOR), Darouich, Sihem3 (AUTHOR) Sihem.Darouich@free.fr, Masmoudi, Aida4 (AUTHOR), Gordon, David5 (AUTHOR), Zender, Gloria1 (AUTHOR), Han, Zhe6 (AUTHOR), Fitzgerald-Butt, Sara1,2,7 (AUTHOR), White, Peter5,7 (AUTHOR), McBride, Kim L.1,2,7 (AUTHOR), Kharrat, Maher3 (AUTHOR), Garg, Vidu1,2,7,8 (AUTHOR) Sihem.Darouich@free.fr
Source: PLoS Genetics. 5/26/2020, Vol. 16 Issue 5, p1-21. 21p.
Database: Academic Search Ultimate
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        Value: 10.1371/journal.pgen.1008639
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              Text: 5/26/2020
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