Welzel, T.;                     Oefelein, L.;                     Holzer, U.;                     Müller, A.;                     Menden, B.;                     Haack, T.B.;                     Groβ, M.;                     Kuemmerle-Deschner, J.B.    
        Variant in the PLCG2 Gene May Cause a Phenotypic Overlap of APLAID/PLAID: Case Series and Literature Review. J. Clin. Med. 2022, 11, 4369.
    https://doi.org/10.3390/jcm11154369
    AMA Style
    
                                Welzel T,                                 Oefelein L,                                 Holzer U,                                 Müller A,                                 Menden B,                                 Haack TB,                                 Groβ M,                                 Kuemmerle-Deschner JB.        
                Variant in the PLCG2 Gene May Cause a Phenotypic Overlap of APLAID/PLAID: Case Series and Literature Review. Journal of Clinical Medicine. 2022; 11(15):4369.
        https://doi.org/10.3390/jcm11154369
    
    Chicago/Turabian Style
    
                                Welzel, Tatjana,                                 Lea Oefelein,                                 Ursula Holzer,                                 Amelie Müller,                                 Benita Menden,                                 Tobias B. Haack,                                 Miriam Groβ,                                 and Jasmin B. Kuemmerle-Deschner.        
                2022. "Variant in the PLCG2 Gene May Cause a Phenotypic Overlap of APLAID/PLAID: Case Series and Literature Review" Journal of Clinical Medicine 11, no. 15: 4369.
        https://doi.org/10.3390/jcm11154369
    
    APA Style
    
                                Welzel, T.,                                 Oefelein, L.,                                 Holzer, U.,                                 Müller, A.,                                 Menden, B.,                                 Haack, T. B.,                                 Groβ, M.,                                 & Kuemmerle-Deschner, J. B.        
        
        (2022). Variant in the PLCG2 Gene May Cause a Phenotypic Overlap of APLAID/PLAID: Case Series and Literature Review. Journal of Clinical Medicine, 11(15), 4369.
        https://doi.org/10.3390/jcm11154369