A new patient with congenital myasthenic syndrome type 20 due to compound heterozygous missense SLC5A7 variants suggests trends in genotype–phenotype correlation. - Vlckova, Marketa; Prchalova, Darina; Zimmermann, Pavel; Haberlova, Jana; Bendova, Sarka; Moslerova, Veronika; Stranecky, Viktor; Sedlacek, Zdenek; Hancarova, Miroslava (Molecular Genetics & Genomic Medicine, 2023)