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Oxford nanopore sequencing-based assay for BTD gene screening: Design, clinical validation, and variant frequency assessment in the Turkish population

Gene. 2024 Jul 19:148782. doi: 10.1016/j.gene.2024.148782. Online ahead of print. ABSTRACT Biotinidase deficiency (BTD) is an autosomal recessive disorder characterized by impaired recycling of the …

Antiarrhythmic therapy for narrow QRS supraventricular tachyarrhythmias in newborns and infants in the first year of life: potent tools to be handled with care

Indian Pacing Electrophysiol J. 2024 Jul 19:S0972-6292(24)00109-8. doi: 10.1016/j.ipej.2024.07.005. Online ahead of print. ABSTRACT Supraventricular tachyarrhythmias pose a significant challenge in neonates and infants, particularly …