Robinson, H. K., Zaklyazminskaya, E., Povolotskaya, I., Surikova, Y., Mallin, L., Armstrong, C., … Ellard, S. (2020). Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy. In EUROPEAN JOURNAL OF HUMAN GENETICS (Vol. 28, pp. 281–282).

Robinson, H. K., E. Zaklyazminskaya, I. Povolotskaya, Y. Surikova, L. Mallin, C. Armstrong, M. R. Chrisant, et al. “Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy.” In EUROPEAN JOURNAL OF HUMAN GENETICS, 28:281–82, 2020.

Robinson HK, Zaklyazminskaya E, Povolotskaya I, Surikova Y, Mallin L, Armstrong C, et al. Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy. In: EUROPEAN JOURNAL OF HUMAN GENETICS. 2020. p. 281–2.

Robinson, H. K., et al. “Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy.” EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 28, no. SUPPL 1, 2020, pp. 281–82.

Robinson HK, Zaklyazminskaya E, Povolotskaya I, Surikova Y, Mallin L, Armstrong C, Chrisant MR, Benke PJ, McDonald M, Marboe CC, McWalter K, Douglas G, Agre K, Deyle D, Balashova KM, Kaimonov V, Shirokova N, Pomerantseva E, Turner C, Ellard S. Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy. EUROPEAN JOURNAL OF HUMAN GENETICS. 2020. p. 281–282.