Association of single nucleotide polymorphisms in PPAR gamma with osteoporosis
摘要
The current invention is based on the discovery that the Pro12A1a and VN102 single nucleotide polymorphisms in the PPAR³2 provides a method of determining a susceptibility to osteoporosis by detecting the presence of PPAR³ of the alleles.
申请公布号
EP1612279(B1)
申请公布日期
2009.03.11
申请号
EP20050013826
申请日期
2005.06.27
申请人
ROCHE DIAGNOSTICS GMBH;F. HOFFMANN-LA ROCHE AG
发明人
HIGUCHI, RUSSELL GENE;LI, JIA;PELTZ, GARY ALLEN;RO, SUNSHEE KWON
