CDC73 Intragenic Deletion in Familial Primary Hyperparathyroidism Associated With Parathyroid Carcinoma

CONTEXT: CDC73 mutations frequently underlie the hyperparathyroidism-jaw tumor syndrome, familial isolated hyperparathyroidism (FIHP), and parathyroid carcinoma. It has also been suggested that CDC73 deletion analysis should be performed in those patients without CDC73 mutations. OBJECTIVE: To inves...

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Bibliografiset tiedot
Päätekijät: Korpi-Hyövälti, Eeva, Cranston, Treena, Ryhänen, Eeva, Arola, Johanna, Aittomäki, Kristiina, Sane, Timo, Thakker, Rajesh V., Schalin-Jäntti, Camilla
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Endocrine Society 2014
Aiheet:
Special Features
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4207936/
https://ncbi.nlm.nih.gov/pubmed/24823466
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2014-1481
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