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Heterozygosity for a coding SNP in COL1A2 confers a lower BMD and an increased stroke risk.
Lindahl K, Rubin CJ, Brändström H, Karlsson MK, Holmberg A, Ohlsson C, Mellström D, Orwoll E, Mallmin H, Kindmark A, Ljunggren O. Lindahl K, et al. Among authors: mellstrom d. Biochem Biophys Res Commun. 2009 Jul 10;384(4):501-5. doi: 10.1016/j.bbrc.2009.05.006. Epub 2009 May 6. Biochem Biophys Res Commun. 2009. PMID: 19426706
The COMT val158met polymorphism is associated with peak BMD in men.
Lorentzon M, Eriksson AL, Mellström D, Ohlsson C. Lorentzon M, et al. Among authors: mellstrom d. J Bone Miner Res. 2004 Dec;19(12):2005-11. doi: 10.1359/JBMR.040909. Epub 2004 Sep 20. J Bone Miner Res. 2004. PMID: 15537444 Free article.
394 results