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APA Citation
Angius, A., Cossu, S., Uva, P., Oppo, M., Onano, S., Persico, I., Fotia, G., Atzeni, R., Cuccuru, G., Asunis, M., Cucca, F., Pruna, D., & Crisponi, L. (2018). novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome. Clinical genetics, 93(6), 1245–1247. http://access.bl.uk/ark:/81055/vdc_100063895002.0x000063