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Clinically relevant intronic splicing enhancer mutation in myelin proteolipid protein leads to progressive microglia and astrocyte activation in white and gray matter regions of the brain
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References
Kenwrick, S. et al. Hum. Genet. 73, 264–266 (1986).
Keppen, L.D. et al. Am. J. hum. Genet. 41, 933–943 (1987).
Jouet, M. et al. Nature Genet. 7, 402–407 (1994).
Vits, L. et al. Nature Genet. 7, 408–413 (1994).
Johnston, A.W. & McKusick, V.A. Am. J. hum. Genet. 14, 83–94 (1962).
Ellis, D. & Malcolm, S. Nature Genet. 6, 333–334 (1994).
Aubourg, P. Nature Genet. 5, 105–106 (1993).
Saugier-Veber, P. et al. Nature Genet. 6, 257–262 (1994).
Schneider, A. et al. Nature 358, 758–761 (1992).
Griffiths, I.R. et al. J. Neurocytol. 19, 273–283 (1990).
Fanarraga, M. et al. Glia 5, 161–170 (1992).
Suter, U., Welcher, A.A. & Snipes, G.J. Trends Neurosci. 16, 50–56 (1993).
Readhead, C., Schneider, A., Griffiths, I. & Nave, K.-A. Neuron 12, 583–595 (1994).
Patel, P.I. & Lupski, J.R. Trends Genet. 10, 128–133 (1994).
Valentijn, L.J. et al. Nature Genet. 2, 288–291 (1992).
Strautnieks, S., Rutland, P., Winter, R.M., Baraitser, M. & Malcolm, S. Am. J. hum. Genet. 51, 871–878 (1992).
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Kobayashi, H., Hoffman, E. & Marks, H. The rumpshaker mutation in spastic paraplegia. Nat Genet 7, 351–352 (1994). https://doi.org/10.1038/ng0794-351
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DOI: https://doi.org/10.1038/ng0794-351
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