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Clinical profile and mutation spectrum of long QT syndrome in Saudi Arabia: The impact of consanguinity.
Heart Rhythm. 2017 Aug;14(8):1191-1199. doi: 10.1016/j.hrthm.2017.04.028. Epub 2017 Apr 22.
Heart Rhythm. 2017.
PMID: 28438721
The Phenotype and Outcome of Infantile Cardiomyopathy Caused by a Homozygous ELAC2 Mutation.
Shinwari ZMA, Almesned A, Alakhfash A, Al-Rashdan AM, Faqeih E, Al-Humaidi Z, Alomrani A, Alghamdi M, Colak D, Alwadai A, Rababh M, Al-Fayyadh M, Al-Hassnan ZN.
Shinwari ZMA, et al. Among authors: rababh m.
Cardiology. 2017;137(3):188-192. doi: 10.1159/000465516. Epub 2017 Apr 26.
Cardiology. 2017.
PMID: 28441660
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A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy.
Al-Hassnan ZN, Shinwari ZM, Wakil SM, Tulbah S, Mohammed S, Rahbeeni Z, Alghamdi M, Rababh M, Colak D, Kaya N, Al-Fayyadh M, Alburaiki J.
Al-Hassnan ZN, et al. Among authors: rababh m.
BMC Med Genet. 2016 Jan 14;17:3. doi: 10.1186/s12881-016-0267-5.
BMC Med Genet. 2016.
PMID: 26768247
Free PMC article.
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Clinical and Genetic Characteristics of Arrhythmogenic Right Ventricular Cardiomyopathy Patients: A Single-Center Experience.
Al-Ghamdi BS, Alhadeq F, Alqahtani A, Alruwaili N, Rababh M, Alghamdi S, Almanea W, Alhassnan Z.
Al-Ghamdi BS, et al. Among authors: rababh m.
Cardiol Res. 2023 Oct;14(5):379-386. doi: 10.14740/cr1531. Epub 2023 Oct 21.
Cardiol Res. 2023.
PMID: 37936624
Free PMC article.
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