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A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding.
van de Meerakker JB, Christiaans I, Barnett P, Lekanne Deprez RH, Ilgun A, Mook OR, Mannens MM, Lam J, Wilde AA, Moorman AF, Postma AV. van de Meerakker JB, et al. Among authors: lam j. Biochim Biophys Acta. 2013 Apr;1833(4):833-9. doi: 10.1016/j.bbamcr.2012.11.003. Epub 2012 Nov 9. Biochim Biophys Acta. 2013. PMID: 23147248 Free article.
The ambiguous role of NKX2-5 mutations in thyroid dysgenesis.
van Engelen K, Mommersteeg MT, Baars MJ, Lam J, Ilgun A, van Trotsenburg AS, Smets AM, Christoffels VM, Mulder BJ, Postma AV. van Engelen K, et al. Among authors: lam j. PLoS One. 2012;7(12):e52685. doi: 10.1371/journal.pone.0052685. Epub 2012 Dec 28. PLoS One. 2012. PMID: 23285148 Free PMC article.
Vascular endothelial growth factor gene haplotypes in Kawasaki disease.
Breunis WB, Biezeveld MH, Geissler J, Ottenkamp J, Kuipers IM, Lam J, Hutchinson A, Welch R, Chanock SJ, Kuijpers TW. Breunis WB, et al. Among authors: lam j. Arthritis Rheum. 2006 May;54(5):1588-94. doi: 10.1002/art.21811. Arthritis Rheum. 2006. PMID: 16645995 Free article.
2,721 results