Cornejo-Sanchez, D.M.;                     Acharya, A.;                     Bharadwaj, T.;                     Marin-Gomez, L.;                     Pereira-Gomez, P.;                     Nouel-Saied, L.M.;                     University of Washington Center for Mendelian Genomics;                     Nickerson, D.A.;                     Bamshad, M.J.;                     Mefford, H.C.;     
    et al.    SCN1A Variants as the Underlying Cause of Genetic Epilepsy with Febrile Seizures Plus in Two Multi-Generational Colombian Families. Genes 2022, 13, 754.
    https://doi.org/10.3390/genes13050754
    AMA Style
    
                                Cornejo-Sanchez DM,                                 Acharya A,                                 Bharadwaj T,                                 Marin-Gomez L,                                 Pereira-Gomez P,                                 Nouel-Saied LM,                                 University of Washington Center for Mendelian Genomics,                                 Nickerson DA,                                 Bamshad MJ,                                 Mefford HC,         
        et al.        SCN1A Variants as the Underlying Cause of Genetic Epilepsy with Febrile Seizures Plus in Two Multi-Generational Colombian Families. Genes. 2022; 13(5):754.
        https://doi.org/10.3390/genes13050754
    
    Chicago/Turabian Style
    
                                Cornejo-Sanchez, Diana M.,                                 Anushree Acharya,                                 Thashi Bharadwaj,                                 Lizeth Marin-Gomez,                                 Pilar Pereira-Gomez,                                 Liz M. Nouel-Saied,                                 University of Washington Center for Mendelian Genomics,                                 Deborah A. Nickerson,                                 Michael J. Bamshad,                                 Heather C. Mefford,         
         and et al.        2022. "SCN1A Variants as the Underlying Cause of Genetic Epilepsy with Febrile Seizures Plus in Two Multi-Generational Colombian Families" Genes 13, no. 5: 754.
        https://doi.org/10.3390/genes13050754
    
    APA Style
    
                                Cornejo-Sanchez, D. M.,                                 Acharya, A.,                                 Bharadwaj, T.,                                 Marin-Gomez, L.,                                 Pereira-Gomez, P.,                                 Nouel-Saied, L. M.,                                 University of Washington Center for Mendelian Genomics,                                 Nickerson, D. A.,                                 Bamshad, M. J.,                                 Mefford, H. C.,                                 Schrauwen, I.,                                 Carrizosa-Moog, J.,                                 Cornejo-Ochoa, W.,                                 Pineda-Trujillo, N.,                                 & Leal, S. M.        
        
        (2022). SCN1A Variants as the Underlying Cause of Genetic Epilepsy with Febrile Seizures Plus in Two Multi-Generational Colombian Families. Genes, 13(5), 754.
        https://doi.org/10.3390/genes13050754