APA (7th ed.) Citation

Vlckova, M., Prchalova, D., Zimmermann, P., Haberlova, J., Bendova, S., Moslerova, V., . . . Hancarova, M. (2023). A new patient with congenital myasthenic syndrome type 20 due to compound heterozygous missense SLC5A7 variants suggests trends in genotype–phenotype correlation. Molecular Genetics & Genomic Medicine, 11(6), 1. https://doi.org/10.1002/mgg3.2154

Chicago Style (17th ed.) Citation

Vlckova, Marketa, Darina Prchalova, Pavel Zimmermann, Jana Haberlova, Sarka Bendova, Veronika Moslerova, Viktor Stranecky, Zdenek Sedlacek, and Miroslava Hancarova. "A New Patient with Congenital Myasthenic Syndrome Type 20 Due to Compound Heterozygous Missense SLC5A7 Variants Suggests Trends in Genotype–phenotype Correlation." Molecular Genetics & Genomic Medicine 11, no. 6 (2023): 1. https://doi.org/10.1002/mgg3.2154.

MLA (9th ed.) Citation

Vlckova, Marketa, et al. "A New Patient with Congenital Myasthenic Syndrome Type 20 Due to Compound Heterozygous Missense SLC5A7 Variants Suggests Trends in Genotype–phenotype Correlation." Molecular Genetics & Genomic Medicine, vol. 11, no. 6, 2023, p. 1, https://doi.org/10.1002/mgg3.2154.