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A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect.

dc.contributor.authorKUCUKEMRE, B
dc.contributor.authorSAGLAM, Yavuz
dc.contributor.authorCANGUL, H
dc.contributor.authorKENDALL, M
dc.contributor.authorDarendeliler, Fatma Feyza
dc.contributor.authorBOELAERT, K
dc.contributor.authorBARRETT, TG
dc.contributor.authorMAHER, ER
dc.date.accessioned2021-03-06T09:09:21Z
dc.date.available2021-03-06T09:09:21Z
dc.identifier.citationCANGUL H., Darendeliler F. F. , SAGLAM Y., KUCUKEMRE B., KENDALL M., BOELAERT K., BARRETT T., MAHER E., "A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect.", Endocrine research, cilt.40, ss.146-50, 2015
dc.identifier.issn0743-5800
dc.identifier.othervv_1032021
dc.identifier.otherav_e45aa011-b824-49df-93d6-9f939b54a0ad
dc.identifier.urihttp://hdl.handle.net/20.500.12627/150263
dc.identifier.urihttps://doi.org/10.3109/07435800.2014.967354
dc.language.isoeng
dc.titleA truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect.
dc.typeMakale
dc.relation.journalEndocrine research
dc.contributor.department, ,
dc.identifier.volume40
dc.identifier.startpage146
dc.identifier.endpage50
dc.contributor.firstauthorID125241


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