Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Andrea Sánchez-Mira"'
Autor:
Ana Beatriz Sánchez-Heras, Estela Dámaso, Adela Castillejo, Mercedes Robledo, Alexandre Teulé, Conxi Lázaro, Rosario Sánchez-Martínez, Ángel Zúñiga, Adrià López-Fernández, Judith Balmaña, Luis Robles, Teresa Ramon y Cajal, M. Isabel Castillejo, Raquel Perea Ibañez, Carmen Martínez Sevila, Andrea Sánchez-Mira, Inés Escandell, Luís Gómez, Pere Berbel, José Luis Soto
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-7 (2024)
Abstract Background Hereditary leiomyomatosis and renal cell cancer syndrome is a rare autosomal dominant hereditary syndrome. Previously, we published the largest cohort of FH mutation carriers in Spain and observed a highly recurrent missense heter
Externí odkaz:
https://doaj.org/article/070bf76381b143af84d1c37cc2907316
Autor:
Sánchez-Heras, Ana Beatriz1 (AUTHOR) sanchez_ana@gva.es, Dámaso, Estela2,3 (AUTHOR), Castillejo, Adela2,3 (AUTHOR), Robledo, Mercedes4,5 (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. Isabel2,3 (AUTHOR), Ibañez, Raquel Perea1 (AUTHOR), Sevila, Carmen Martínez1 (AUTHOR), Sánchez-Mira, Andrea2,3 (AUTHOR), Escandell, Inés12 (AUTHOR), Gómez, Luís13 (AUTHOR), Berbel, Pere14 (AUTHOR), Soto, José Luis2,3 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 1/26/2024, Vol. 19 Issue 1, p1-7. 7p.