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Page 1
Molecular modeling of disease causing mutations in domain C1 of cMyBP-C.
Gajendrarao P, Krishnamoorthy N, Kassem HSh, Moharem-Elgamal S, Cecchi F, Olivotto I, Yacoub MH. Gajendrarao P, et al. Among authors: kassem hsh. PLoS One. 2013;8(3):e59206. doi: 10.1371/journal.pone.0059206. Epub 2013 Mar 19. PLoS One. 2013. PMID: 23527136 Free PMC article.
New Variant With a Previously Unrecognized Mechanism of Pathogenicity in Hypertrophic Cardiomyopathy.
Aguib Y, Allouba M, Walsh R, Ibrahim AM, Halawa S, Afify A, Hosny M, Theotokis PI, Galal A, Elshorbagy S, Roshdy M, Kassem HS, Ellithy A, Buchan R, Whiffin N, Anwer S, Cook SA, Moustafa A, ElGuindy A, Ware JS, Barton PJR, Yacoub M. Aguib Y, et al. Circulation. 2021 Aug 31;144(9):754-757. doi: 10.1161/CIRCULATIONAHA.120.048295. Epub 2021 Aug 30. Circulation. 2021. PMID: 34460321 Free PMC article. No abstract available.
Molecular genetics made simple.
Kassem HSh, Girolami F, Sanoudou D. Kassem HSh, et al. Glob Cardiol Sci Pract. 2012 Jul 4;2012(1):6. doi: 10.5339/gcsp.2012.6. eCollection 2012. Glob Cardiol Sci Pract. 2012. PMID: 25610837 Free PMC article. Review.