Mukherjee, O., Pastor, P., Cairns, N. J., Chakraverty, S., Kauwe, J. S. K., Shears, S., . . . Goate, A. M. (2006). HDDD2 Is a Familial Frontotemporal Lobar Degeneration with Ubiquitin-Positive, Tau-Negative Inclusions Caused by a Missense Mutation in the Signal Peptide of Progranulin.
Chicago-tyylinen lähdeviittausMukherjee, Odity, et al. HDDD2 Is a Familial Frontotemporal Lobar Degeneration With Ubiquitin-Positive, Tau-Negative Inclusions Caused By a Missense Mutation in the Signal Peptide of Progranulin. 2006.
MLA-viiteMukherjee, Odity, et al. HDDD2 Is a Familial Frontotemporal Lobar Degeneration With Ubiquitin-Positive, Tau-Negative Inclusions Caused By a Missense Mutation in the Signal Peptide of Progranulin. 2006.
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