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dc.contributor.authorGadelha, MRen_US
dc.contributor.authorKasuki, Len_US
dc.contributor.authorKorbonits, Men_US
dc.date.accessioned2017-03-21T13:34:07Z
dc.date.available2017-01-03en_US
dc.date.issued2017-02en_US
dc.date.submitted2017-02-28T05:03:59.858Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/21959
dc.description.abstractAcromegaly is caused by a somatotropinoma in the vast majority of the cases. These are monoclonal tumors that can occur sporadically or rarely in a familial setting. In the last few years, novel familial syndromes have been described and recent studies explored the landscape of somatic mutations in sporadic somatotropinomas. This short review concentrates on the current knowledge of the genetic basis of both familial and sporadic acromegaly.en_US
dc.format.extent10 - 21en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofPituitaryen_US
dc.rights“The final publication is available at Springer via http://dx.doi.org/10.1007/s11102-017-0789-7”
dc.subjectAIPen_US
dc.subjectAcromegalyen_US
dc.subjectFamilial diseaseen_US
dc.subjectGenetic basisen_US
dc.subjectAcromegalyen_US
dc.subjectFemaleen_US
dc.subjectGenetic Backgrounden_US
dc.subjectGrowth Hormone-Secreting Pituitary Adenomaen_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectMutationen_US
dc.titleThe genetic background of acromegaly.en_US
dc.typeArticle
dc.rights.holder(c) The Author(s) 2017.
dc.identifier.doi10.1007/s11102-017-0789-7en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/28161730en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume20en_US


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