Rapid Mutation Screening for HRPT2 and MEN1 Mutations Associated with Familial and Sporadic Primary Hyperparathyroidism

Familial hyperparathyroidism, a disease of the parathyroid glands, may occur in conjunction with pituitary and pancreatic tumors (multiple endocrine neoplasia type I), kidney and bone tumors (hyperparathyroidism jaw tumor syndrome), or alone (familial isolated hyperparathyroidism). This study descri...

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Hauptverfasser: Howell, Viive M., Cardinal, John W., Richardson, Anne-Louise, Gimm, Oliver, Robinson, Bruce G., Marsh, Deborah J.
Format: Artigo
Sprache:Inglês
Veröffentlicht: American Society for Investigative Pathology 2006
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Regular Articles
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1876168/
https://ncbi.nlm.nih.gov/pubmed/17065424
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/jmoldx.2006.060015
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