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Exploring the sortilin related receptor, SorLA, in depression.
Buttenschøn HN, Elfving B, Nielsen M, Skeldal S, Kaas M, Mors O, Glerup S. Buttenschøn HN, et al. Among authors: nielsen m. J Affect Disord. 2018 May;232:260-267. doi: 10.1016/j.jad.2018.02.050. Epub 2018 Feb 21. J Affect Disord. 2018. PMID: 29499509
Association between genes on chromosome 19p13.2 and panic disorder.
Gregersen NO, Buttenschøn HN, Hedemand A, Nielsen MN, Dahl HA, Kristensen AS, Johansen O, Woldbye DP, Erhardt A, Kruse TA, Wang AG, Børglum AD, Mors O. Gregersen NO, et al. Psychiatr Genet. 2016 Dec;26(6):287-292. doi: 10.1097/YPG.0000000000000147. Psychiatr Genet. 2016. PMID: 27610895
Heterozygosity for an in-frame deletion causes glutaryl-CoA dehydrogenase deficiency in a patient detected by newborn screening: investigation of the effect of the mutant allele.
Bross P, Frederiksen JB, Bie AS, Hansen J, Palmfeldt J, Nielsen MN, Duno M, Lund AM, Christensen E. Bross P, et al. Among authors: nielsen mn. J Inherit Metab Dis. 2012 Sep;35(5):787-96. doi: 10.1007/s10545-011-9437-y. Epub 2012 Jan 10. J Inherit Metab Dis. 2012. PMID: 22231382
4,675 results