Dias, C., Punetha, J., Zheng, C., Mazaheri, N., Rad, A., Efthymiou, S., . . . Maroofian, R. (2019). Homozygous missense variants in NTNG2, encoding a presynaptic netrin-G2 adhesion protein, lead to a distinct neurodevelopmental disorder. Elsevier.
Citace podle Chicago (17th ed.)Dias, CM, et al. Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. Elsevier, 2019.
Citace podle MLA (9th ed.)Dias, CM, et al. Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. Elsevier, 2019.
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