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SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.
Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):984-92. doi: 10.1002/ajmg.b.30928.
Am J Med Genet B Neuropsychiatr Genet. 2009.
PMID: 19194956
Re-evaluation of the dysequilibrium syndrome.
Melberg A, Orlén H, Raininko R, Entesarian M, Dahlqvist J, Gustavson KH, Dahl N.
Melberg A, et al. Among authors: orlen h.
Acta Neurol Scand. 2011 Jan;123(1):28-33. doi: 10.1111/j.1600-0404.2010.01335.x.
Acta Neurol Scand. 2011.
PMID: 20199520
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Multiple epiphyseal dysplasia.
Dahlqvist J, Orlén H, Matsson H, Dahl N, Lönnerholm T, Gustavson KH.
Dahlqvist J, et al. Among authors: orlen h.
Acta Orthop. 2009 Dec;80(6):711-5. doi: 10.3109/17453670903473032.
Acta Orthop. 2009.
PMID: 19995321
Free PMC article.
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Welander distal myopathy caused by an ancient founder mutation in TIA1 associated with perturbed splicing.
Klar J, Sobol M, Melberg A, Mäbert K, Ameur A, Johansson AC, Feuk L, Entesarian M, Orlén H, Casar-Borota O, Dahl N.
Klar J, et al. Among authors: orlen h.
Hum Mutat. 2013 Apr;34(4):572-7. doi: 10.1002/humu.22282.
Hum Mutat. 2013.
PMID: 23348830
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Weak mutators can drive the evolution of fluoroquinolone resistance in Escherichia coli.
Orlén H, Hughes D.
Orlén H, et al.
Antimicrob Agents Chemother. 2006 Oct;50(10):3454-6. doi: 10.1128/AAC.00783-06.
Antimicrob Agents Chemother. 2006.
PMID: 17005830
Free PMC article.
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