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A novel homozygous TPM1 mutation in familial pediatric hypertrophic cardiomyopathy and in silico screening of potential targeting drugs.
Carlus SJ, Almuzaini IS, Karthikeyan M, Loganathan L, Al-Harbi GS, Carlus FH, Al-Mazroea AH, Morsy MM, Abo-Haded HM, Abdallah AM, Al-Harbi KM. Carlus SJ, et al. Among authors: almuzaini is. Eur Rev Med Pharmacol Sci. 2020 Jul;24(14):7732-7744. doi: 10.26355/eurrev_202007_22299. Eur Rev Med Pharmacol Sci. 2020. PMID: 32744700 Free article.