Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Geoffroy J P E Goujon"'
Autor:
Hans-Jurgen J Mager, Sabrina Martin, Georgios Galaris, Geoffroy J P E Goujon, Ton J. Rabelink, Franck Lebrin, Kevin Montagne, Sander van den Driesche, Jérémy H. Thalgott, Christine L. Mummery
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 16
International Journal of Molecular Sciences, Vol 22, Iss 8948, p 8948 (2021)
International Journal of Molecular Sciences, 22(16). MDPI
Volume 22
Issue 16
International Journal of Molecular Sciences, Vol 22, Iss 8948, p 8948 (2021)
International Journal of Molecular Sciences, 22(16). MDPI
Hereditary Hemorrhagic Telangiectasia type 1 (HHT1) is an autosomal dominant inherited disease characterized by arteriovenous malformations and hemorrhage. HHT1 is caused by mutations in ENDOGLIN, which encodes an ancillary receptor for Transforming
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b23fc17f86412ab0d75871405c016ed3
Autor:
Galaris, Georgios1 (AUTHOR) G.Galaris@lumc.nl, Montagne, Kévin2 (AUTHOR) montagne@m.u-tokyo.ac.jp, Thalgott, Jérémy H.1 (AUTHOR) J.H.Thalgott@lumc.nl, Goujon, Geoffroy J. P. E.1 (AUTHOR) G.J.P.E.Goujon@lumc.nl, van den Driesche, Sander3,4 (AUTHOR) S.vandenDriesche@ed.ac.uk, Martin, Sabrina5 (AUTHOR) Sabrina.martin@college-de-france.fr, Mager, Hans-Jurgen J.6 (AUTHOR) j.mager@antoniusziekenhuis.nl, Mummery, Christine L.7 (AUTHOR) C.L.Mummery@lumc.nl, Rabelink, Ton J.1 (AUTHOR) A.J.Rabelink@lumc.nl, Lebrin, Franck1,8,9 (AUTHOR) f.lebrin@lumc.nl
Publikováno v:
International Journal of Molecular Sciences. Aug2021, Vol. 22 Issue 16, p8948-8948. 1p.