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Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.
Bdier AY, Al-Ghamdi S, Verma PK, Dagriri K, Alshehri B, Jiman OA, Ahmed SE, Wilde AAM, Bhuiyan ZA, Al-Aama JY. Bdier AY, et al. Among authors: bhuiyan za. Mol Genet Genomic Med. 2017 Jun 21;5(5):592-601. doi: 10.1002/mgg3.305. eCollection 2017 Sep. Mol Genet Genomic Med. 2017. PMID: 28944242 Free PMC article.
Genetic Mosaicism in Calmodulinopathy.
Wren LM, Jiménez-Jáimez J, Al-Ghamdi S, Al-Aama JY, Bdeir A, Al-Hassnan ZN, Kuan JL, Foo RY, Potet F, Johnson CN, Aziz MC, Carvill GL, Kaski JP, Crotti L, Perin F, Monserrat L, Burridge PW, Schwartz PJ, Chazin WJ, Bhuiyan ZA, George AL Jr. Wren LM, et al. Among authors: bhuiyan za. Circ Genom Precis Med. 2019 Sep;12(9):375-385. doi: 10.1161/CIRCGEN.119.002581. Epub 2019 Aug 27. Circ Genom Precis Med. 2019. PMID: 31454269 Free PMC article.
TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT.
Devalla HD, Gélinas R, Aburawi EH, Beqqali A, Goyette P, Freund C, Chaix MA, Tadros R, Jiang H, Le Béchec A, Monshouwer-Kloots JJ, Zwetsloot T, Kosmidis G, Latour F, Alikashani A, Hoekstra M, Schlaepfer J, Mummery CL, Stevenson B, Kutalik Z, de Vries AA, Rivard L, Wilde AA, Talajic M, Verkerk AO, Al-Gazali L, Rioux JD, Bhuiyan ZA, Passier R. Devalla HD, et al. Among authors: bhuiyan za. EMBO Mol Med. 2016 Dec 1;8(12):1390-1408. doi: 10.15252/emmm.201505719. Print 2016 Dec. EMBO Mol Med. 2016. PMID: 27861123 Free PMC article.
Discordance Between Germline and Blood Mosaicism in Calmodulinopathy.
Bhuiyan ZA, Bdier A, Al-Aama JY, Abramova T, George AL Jr. Bhuiyan ZA, et al. Circ Genom Precis Med. 2022 Aug;15(4):e003695. doi: 10.1161/CIRCGEN.121.003695. Epub 2022 May 11. Circ Genom Precis Med. 2022. PMID: 35543700 No abstract available.
88 results