Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient's phenotype?
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Published in Frontiers in genetics (09.01.2023)
Published in Frontiers in genetics (09.01.2023)
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Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction
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Published in Advances in clinical and experimental medicine : official organ Wroclaw Medical University (01.04.2020)
Published in Advances in clinical and experimental medicine : official organ Wroclaw Medical University (01.04.2020)
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Journal Article
Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient's phenotype?
Touhami, Rahma, Foddha, Hajer, Alix, Eudeline, Jalloul, Afef, Mougou-Zerelli, Soumaya, Saad, Ali, Sanlaville, Damien, Haj Khelil, Amel
Published in Frontiers in genetics (01.01.2022)
Published in Frontiers in genetics (01.01.2022)
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