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Autor:
Victoria Campuzano, Maria Segura-Puimedon, Verena Terrado, Carolina Sánchez-Rodríguez, Mathilde Coustets, Mauricio Menacho-Márquez, Julián Nevado, Xosé R Bustelo, Uta Francke, Luis A Pérez-Jurado
Publikováno v:
PLoS Genetics, Vol 8, Iss 2, p e1002458 (2012)
A hallmark feature of Williams-Beuren Syndrome (WBS) is a generalized arteriopathy due to elastin deficiency, presenting as stenoses of medium and large arteries and leading to hypertension and other cardiovascular complications. Deletion of a functi
Externí odkaz:
https://doaj.org/article/4199344e2bde496e817d2ba41ec1da8f
Autor:
Uta Francke, Xosé R. Bustelo, Mauricio Menacho-Márquez, Victoria Campuzano, Mathilde Coustets, Carolina Sánchez-Rodríguez, Verena Terrado, Luis A. Pérez-Jurado, Maria Segura-Puimedon, Julián Nevado
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
PLoS Genetics, Vol 8, Iss 2, p e1002458 (2012)
PLoS Genetics
Digital.CSIC. Repositorio Institucional del CSIC
instname
PLoS Genetics, Vol 8, Iss 2, p e1002458 (2012)
PLoS Genetics
Digital.CSIC. Repositorio Institucional del CSIC
This is an open-access article distributed under the terms of the Creative Commons Attribution License.-- et al.
A hallmark feature of Williams-Beuren Syndrome (WBS) is a generalized arteriopathy due to elastin deficiency, presenting as stenoses
A hallmark feature of Williams-Beuren Syndrome (WBS) is a generalized arteriopathy due to elastin deficiency, presenting as stenoses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ae94d3802fdd44a16156f34b157c92e
http://hdl.handle.net/10230/23439
http://hdl.handle.net/10230/23439