| Literature DB >> 16001331 |
P F Wang1, M-H Tan, C Zhang, H Morreau, B T Teh.
Abstract
Hyperparathyroidism-jaw tumor (HPT-JT) syndrome is a familial multi-tumor syndrome resulting from inactivating mutations in the HRPT2 tumor suppressor gene, which encodes a protein product named parafibromin. Here, we will review recent advances in genetic and protein studies on parafibromin, and examine its biological functions.Entities:
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Year: 2005 PMID: 16001331 DOI: 10.1055/s-2005-870150
Source DB: PubMed Journal: Horm Metab Res ISSN: 0018-5043 Impact factor: 2.936