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Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.
Andersen PS, Havndrup O, Bundgaard H, Moolman-Smook JC, Larsen LA, Mogensen J, Brink PA, Børglum AD, Corfield VA, Kjeldsen K, Vuust J, Christiansen M. Andersen PS, et al. Among authors: borglum ad. J Med Genet. 2001 Dec;38(12):E43. doi: 10.1136/jmg.38.12.e43. J Med Genet. 2001. PMID: 11748309 Free PMC article. No abstract available.
Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy.
Mogensen J, Perrot A, Andersen PS, Havndrup O, Klausen IC, Christiansen M, Bross P, Egeblad H, Bundgaard H, Osterziel KJ, Haltern G, Lapp H, Reinecke P, Gregersen N, Børglum AD. Mogensen J, et al. Among authors: borglum ad. J Med Genet. 2004 Jan;41(1):e10. doi: 10.1136/jmg.2003.010447. J Med Genet. 2004. PMID: 14729850 Free PMC article. No abstract available.
CACNA1C (rs1006737) is associated with schizophrenia.
Nyegaard M, Demontis D, Foldager L, Hedemand A, Flint TJ, Sørensen KM, Andersen PS, Nordentoft M, Werge T, Pedersen CB, Hougaard DM, Mortensen PB, Mors O, Børglum AD. Nyegaard M, et al. Among authors: borglum ad. Mol Psychiatry. 2010 Feb;15(2):119-21. doi: 10.1038/mp.2009.69. Mol Psychiatry. 2010. PMID: 20098439 No abstract available.
370 results