L. Minarik
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Hereditary Haemorrhagic Telangiectasia (HHT) Marked by ACVRL1C1120T Variant Displays Hypopigmented Naevi and Frequent Bleeding Episodes if CYP2C9 Co-Mutated: Clinical Notes & Rationale of Patient Registry
L. Minarik, K. Vargova, N. Dusilkova, V. Kulvait, A. Jonasova, O. Kodet, Tomas Stopka
2020, Vol. 66, Issue 1, pp. 1-6