Relevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical management

dc.contributor.author	Hermsen, Mario
dc.contributor.author	Sevilla García, María Agustina
dc.contributor.author	Llorente Pendás, José Luis
dc.contributor.author	Weiss, Marjan M.
dc.contributor.author	Grimbergen, Anneliese E. M.
dc.contributor.author	Allonca Campa, Eva
dc.contributor.author	García Inclán, Cristina
dc.contributor.author	Balbín Felechosa, Milagros
dc.contributor.author	Suárez Nieto, Carlos
dc.date.accessioned	2016-03-22T13:15:51Z
dc.date.available	2016-03-22T13:15:51Z
dc.date.issued	2010
dc.identifier.citation	Cellular Oncology, 32(4), p. 275-283 (2010); doi:10.3233/CLO-2009-0498
dc.identifier.issn	1570-5870
dc.identifier.uri	http://hdl.handle.net/10651/36175
dc.format.extent	p. 275-283
dc.language.iso	eng
dc.relation.ispartof	Cellular Oncology
dc.rights	© 2010 - IOS Press and the authors.
dc.source	Scopus
dc.source.uri	http://www.scopus.com/inward/record.url?eid=2-s2.0-77953449767&partnerID=40&md5=70b360d256e70bd999bbf39c43512243
dc.title	Relevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical management
dc.type	journal article
dc.identifier.doi	10.3233/CLO-2009-0498
dc.relation.publisherversion	http://dx.doi.org/10.3233/CLO-2009-0498

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