Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Motor Neuron Disease and CHMP2B[original query] |
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Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients. European journal of neurology : the official journal of the European Federation of Neurological Societies 2010 Nov 17 (11): 1393-5. Kaivorinne A-L, Krüger J, Udd B, Majamaa K, Remes A |
Genetics of dementia in a Finnish cohort. European journal of human genetics : EJHG 2018 Feb . Pasanen Petra, Myllykangas Liisa, Pöyhönen Minna, Kiviharju Anna, Siitonen Maija, Hardy John, Bras Jose, Paetau Anders, Tienari Pentti J, Guerreiro Rita, Verkkoniemi-Ahola Au |
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