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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Howell, Viive M., Cardinal, John W., Richardson, Anne-Louise, Gimm, Oliver, Robinson, Bruce G., Marsh, Deborah J.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society for Investigative Pathology 2006
Gaiak:
Regular Articles
Sarrera elektronikoa: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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