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Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome.
Evrony GD, Cordero DR, Shen J, Partlow JN, Yu TW, Rodin RE, Hill RS, Coulter ME, Lam AN, Jayaraman D, Gerrelli D, Diaz DG, Santos C, Morrison V, Galli A, Tschulena U, Wiemann S, Martel MJ, Spooner B, Ryu SC, Elhosary PC, Richardson JM, Tierney D, Robinson CA, Chibbar R, Diudea D, Folkerth R, Wiebe S, Barkovich AJ, Mochida GH, Irvine J, Lemire EG, Blakley P, Walsh CA. Evrony GD, et al. Among authors: robinson ca. Genome Res. 2017 Aug;27(8):1323-1335. doi: 10.1101/gr.219899.116. Epub 2017 Jun 19. Genome Res. 2017. PMID: 28630177 Free PMC article.
Parkinsonism, Lrrk2 G2019S, and tau neuropathology.
Rajput A, Dickson DW, Robinson CA, Ross OA, Dächsel JC, Lincoln SJ, Cobb SA, Rajput ML, Farrer MJ. Rajput A, et al. Among authors: robinson ca. Neurology. 2006 Oct 24;67(8):1506-8. doi: 10.1212/01.wnl.0000240220.33950.0c. Neurology. 2006. PMID: 17060589
Neuroleptic-induced Parkinsonism: Clinicopathological study.
Shuaib UA, Rajput AH, Robinson CA, Rajput A. Shuaib UA, et al. Among authors: robinson ca. Mov Disord. 2016 Mar;31(3):360-5. doi: 10.1002/mds.26467. Epub 2015 Dec 11. Mov Disord. 2016. PMID: 26660063 Free PMC article.
Essential tremor is not dependent upon cerebellar Purkinje cell loss.
Rajput AH, Robinson CA, Rajput ML, Robinson SL, Rajput A. Rajput AH, et al. Among authors: robinson ca, robinson sl. Parkinsonism Relat Disord. 2012 Jun;18(5):626-8. doi: 10.1016/j.parkreldis.2012.01.013. Epub 2012 Feb 3. Parkinsonism Relat Disord. 2012. PMID: 22306459
340 results