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Year | Number of Results |
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2004 | 1 |
2006 | 2 |
2024 | 0 |
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Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).
Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2218-23. doi: 10.1167/iovs.03-1413.
Invest Ophthalmol Vis Sci. 2004.
PMID: 15223798
Horizontal gaze palsy with progressive scoliosis can result from compound heterozygous mutations in ROBO3.
Chan WM, Traboulsi EI, Arthur B, Friedman N, Andrews C, Engle EC.
Chan WM, et al.
J Med Genet. 2006 Mar;43(3):e11. doi: 10.1136/jmg.2005.035436.
J Med Genet. 2006.
PMID: 16525029
Free PMC article.
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Diffusion tensor MRI shows abnormal brainstem crossing fibers associated with ROBO3 mutations.
Sicotte NL, Salamon G, Shattuck DW, Hageman N, Rüb U, Salamon N, Drain AE, Demer JL, Engle EC, Alger JR, Baloh RW, Deller T, Jen JC.
Sicotte NL, et al.
Neurology. 2006 Aug 8;67(3):519-21. doi: 10.1212/01.wnl.0000227960.38262.0c.
Neurology. 2006.
PMID: 16894121
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