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

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Bibliographic Details
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, Sara^1,2,7 (AUTHOR), White, Peter^5,7 (AUTHOR), McBride, Kim L.^1,2,7 (AUTHOR), Kharrat, Maher³ (AUTHOR), Garg, Vidu^1,2,7,8 (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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Description
ISSN:	15537390
DOI:	10.1371/journal.pgen.1008639