D’Souza, I., Poorkaj, P., Hong, M., Nochlin, D., Lee, V. M., Bird, T. D., & Schellenberg, G. D. (1999). Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements. The National Academy of Sciences.
Chicago Style aipamenaD’Souza, Ian, Parvoneh Poorkaj, Ming Hong, David Nochlin, Virginia M.-Y Lee, Thomas D. Bird, and Gerard D. Schellenberg. Missense and Silent Tau Gene Mutations Cause Frontotemporal Dementia With Parkinsonism-chromosome 17 Type, By Affecting Multiple Alternative RNA Splicing Regulatory Elements. The National Academy of Sciences, 1999.
MLA aipamenaD’Souza, Ian, et al. Missense and Silent Tau Gene Mutations Cause Frontotemporal Dementia With Parkinsonism-chromosome 17 Type, By Affecting Multiple Alternative RNA Splicing Regulatory Elements. The National Academy of Sciences, 1999.