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Penetrance and clinical features of pheochromocytoma in a six-generation family carrying a germline TMEM127 mutation.\n                      J Clin Endocrinol Metab\n                      . 2015;100:E308\u201318.","DOI":"10.1210\/jc.2014-2473"},{"key":"ref8","doi-asserted-by":"crossref","unstructured":"Neumann HP, Sullivan M, Winter A, et al. Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sites.\n                      J Clin Endocrinol Metab\n                      . 2011;96:E1279\u201382.","DOI":"10.1210\/jc.2011-0114"},{"key":"ref9","doi-asserted-by":"crossref","unstructured":"Vicha A, Musil Z, Pacak K. 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Novel TMEM127 variant associated to bilateral phaeochromocytoma with an uncommon clinical presentation.\n                      Case Rep Endocrinol\n                      . 2019;2019:2502174.","DOI":"10.1155\/2019\/2502174"}],"container-title":["European Endocrinology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/touchendocrinology.com\/endocrine-oncology\/journal-articles\/pheochromocytoma-due-to-tmem127-mutation-the-importance-of-genetic-testing-for-clinical-decision\/","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,12,3]],"date-time":"2025-12-03T06:59:51Z","timestamp":1764745191000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.touchendocrinology.com\/pheochromocytoma-due-to-tmem127-mutation-the-importance-of-genetic-testing-for-clinical-decision\/"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020]]},"references-count":11,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2020]]}},"alternative-id":["EE.2020.16.1.72"],"URL":"https:\/\/doi.org\/10.17925\/ee.2020.16.1.72","relation":{},"ISSN":["1758-3772"],"issn-type":[{"type":"print","value":"1758-3772"}],"subject":[],"published":{"date-parts":[[2020]]}}}