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Angiotensin-converting enzyme gene insertion/deletion polymorphism in Saudi patients with rheumatic heart disease.
Saudi Med J. 2015 Feb;36(2):176-80. doi: 10.15537/smj.2015.2.10267.
Saudi Med J. 2015.
PMID: 25719581
Free PMC article.
Next-generation sequencing identifies a homozygous mutation in ACADVL associated with pediatric familial dilated cardiomyopathy.
Carlus SJ, Almuzaini IS, Karthikeyan M, Loganathan L, Al-Harbi GS, Abdallah AM, Al-Harbi KM.
Carlus SJ, et al. Among authors: almuzaini is.
Eur Rev Med Pharmacol Sci. 2019 Feb;23(4):1710-1721. doi: 10.26355/eurrev_201902_17133.
Eur Rev Med Pharmacol Sci. 2019.
PMID: 30840296
Free article.
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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.
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