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Majamaa, K.
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Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequ...
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Phenotype of patients with Charcot-Marie-Tooth with the p.His123Arg mutation in...
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Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finn...
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Prehospital and hospital delays for stroke patients treated with thrombolysis:a...
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Childhood hearing impairment in northern Finland:prevalence, aetiology and addit...
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