Pesquisadores descobrem mutação chave que causa DFT e ELA
22 de setembro de 2011
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Researchers find key mutation that causes FTD and ALS: In a landmark paper published in the online journal Neuron today a group of researchers report successful identification of a long-sought mutation that can cause both FTD and ALS. Found in a non-coding region of chromosome 9, this is by far the most common mutation for familial FTD and/or ALS discovered to date. Click here for more information.
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