1. Genetic landscape in Russian patients with familial left ventricular noncompaction
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2. A report of a pedigree with compound heterozygous mutations in the SLC22A5 gene
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3. The role of efflux transporters and metabolizing enzymes in brain and peripheral organs to explain drug‐resistant epilepsy
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4. Clinical and Gene Analysis of Fatty Acid Oxidation Disorders Found in Neonatal Tandem Mass Spectrometry Screening
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