The European Rare Disease Network for HHT Frameworks for management of hereditary haemorrhagic telangiectasia in general and speciality care

Autor:	Shovlin, C.L. a, i, ∗, Buscarini, E. b, ∗∗, Sabbà, C. c, Mager, H.J. d, Kjeldsen, A.D. e, Pagella, F. f, Sure, U. g, j, Ugolini, S. f, Torring, P.M. e, Suppressa, P. c, Rennie, C. a, Post, M.C. d, k, Patel, M.C. a, Nielsen, T.H. e, Manfredi, G. b, Lenato, G.M. c, Lefroy, D. a, Kariholu, U. a, Jones, B. a, Fialla, A.D. e, Eker, O.F. h, Dupuis, O. h, Droege, F. g, l, Coote, N. a, Boccardi, E. b, m, Alsafi, A. a, Alicante, S. b, Dupuis-Girod, S. h, ∗∗∗
Zdroj:	In European Journal of Medical Genetics January 2022 65(1)
Databáze:	ScienceDirect
Externí odkaz:	Zobrazit plný text záznamu Full Text from ScienceDirect