Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene

Autor: Seri, M, Savino, M, Bordo, D, Cusano, R, Rocca, B, Meloni, I, DI BARI, F, Koivisto, Pa, Ravazzolo, Roberto, Renieri, A, Savoia, A.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3710::d766197ef19b35642857a9b5c6636ae5
http://hdl.handle.net/11567/211286

Two percent of Finnish prostate cancer patients have a germ-line mutation in the hormone-binding domain of the androgen receptor gene

Autor: Mononen, N, Syrjäkoski, K, Matikainen, M, Tammela, TLJ, Schleutker, J, Kallioniemi, O-P, Trapman, Jan, Koivisto, PA

Publikováno v: Cancer Research, 60, 6479-6481. American Association for Cancer Research Inc.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=narcis______::0bfd53d81af56a713c795a414b02e1fb
https://pure.eur.nl/en/publications/21e8f8f8-0809-4bd7-9c75-e8d8e71650d9

Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome.

Autor: Sánchez-Heras, Ana Beatriz¹ (AUTHOR) sanchez_ana@gva.es, Dámaso, Estela^2,3 (AUTHOR), Castillejo, Adela^2,3 (AUTHOR), Robledo, Mercedes^4,5 (AUTHOR), Teulé, Alexandre⁶ (AUTHOR), Lázaro, Conxi⁶ (AUTHOR), Sánchez-Martínez, Rosario⁷ (AUTHOR), Zúñiga, Ángel⁸ (AUTHOR), López-Fernández, Adrià⁹ (AUTHOR), Balmaña, Judith⁹ (AUTHOR), Robles, Luis¹⁰ (AUTHOR), Ramon y Cajal, Teresa¹¹ (AUTHOR), Castillejo, M. Isabel^2,3 (AUTHOR), Ibañez, Raquel Perea¹ (AUTHOR), Sevila, Carmen Martínez¹ (AUTHOR), Sánchez-Mira, Andrea^2,3 (AUTHOR), Escandell, Inés¹² (AUTHOR), Gómez, Luís¹³ (AUTHOR), Berbel, Pere¹⁴ (AUTHOR), Soto, José Luis^2,3 (AUTHOR)

Publikováno v: Orphanet Journal of Rare Diseases. 1/26/2024, Vol. 19 Issue 1, p1-7. 7p.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.