Articles with "kif1b v1529m" as a keyword



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A case of juvenile-onset pheochromocytoma with KIF1B p.V1529M germline mutation.

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Published in 2022 at "Endocrine journal"

DOI: 10.1507/endocrj.ej21-0475

Abstract: In 2008, a familial noradrenergic pheochromocytoma (PCC) with a KIF1B germline mutation in exon 41 was reported in a 24-year-old female proband and her family. However, in 2020, the same research group reported that the… read more here.

Keywords: juvenile onset; mutation; kif1b v1529m; germline mutation ... See more keywords