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Mutation ∆K281 in MAPT causes Pick's disease.
Schweighauser M, Garringer HJ, Klingstedt T, Nilsson KPR, Masuda-Suzukake M, Murrell JR, Risacher SL, Vidal R, Scheres SHW, Goedert M, Ghetti B, Newell KL. Schweighauser M, et al. Among authors: murrell jr. Acta Neuropathol. 2023 Aug;146(2):211-226. doi: 10.1007/s00401-023-02598-6. Epub 2023 Jun 23. Acta Neuropathol. 2023. PMID: 37351604 Free PMC article.
Rapid-onset dystonia-parkinsonism associated with the I758S mutation of the ATP1A3 gene: a neuropathologic and neuroanatomical study of four siblings.
Oblak AL, Hagen MC, Sweadner KJ, Haq I, Whitlow CT, Maldjian JA, Epperson F, Cook JF, Stacy M, Murrell JR, Ozelius LJ, Brashear A, Ghetti B. Oblak AL, et al. Among authors: murrell jr. Acta Neuropathol. 2014 Jul;128(1):81-98. doi: 10.1007/s00401-014-1279-x. Epub 2014 May 7. Acta Neuropathol. 2014. PMID: 24803225 Free PMC article.
Cerebral hypometabolism and grey matter density in MAPT intron 10 +3 mutation carriers.
Deters KD, Risacher SL, Farlow MR, Unverzagt FW, Kareken DA, Hutchins GD, Yoder KK, Murrell JR, Spina S, Epperson F, Gao S, Saykin AJ, Ghetti B. Deters KD, et al. Among authors: murrell jr. Am J Neurodegener Dis. 2014 Dec 5;3(3):103-14. eCollection 2014. Am J Neurodegener Dis. 2014. PMID: 25628962 Free PMC article.
155 results