1 | AMACR, AMACRD
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| AMACR mutations cause late-onset autosomal recessive cerebellar ataxia.
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| Dick D, Horvath R, Chinnery PF.
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| Neurology 76(20):1768-70. No abstract available.
2011
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2 | AMACR, AMACRD
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| An adult onset case of alpha-methyl-acyl-CoA racemase deficiency.
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| Smith EH, Gavrilov DK, Oglesbee D, Freeman WD, Vavra MW, Matern D, Tortorelli S.
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| J Inherit Metab Dis 33 Suppl 3:S349-53. doi: 10.1007/s10545-010-9183-6. Epub 2010 Sep 4.
2010
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3 | AMACR, AMACRD
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| Relapsing encephalopathy in a patient with alpha-methylacyl-CoA racemase deficiency.
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| Thompson SA, Calvin J, Hogg S, Ferdinandusse S, Wanders RJ, Barker RA.
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| J Neurol Neurosurg Psychiatry 79(4):448-50. Epub 2007 Nov 21.
2008
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4 | AMACR, AMACRD
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| Mutations in the gene encoding peroxisomal alpha-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy.
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| Ferdinandusse S, Denis S, Clayton PT, Graham A, Rees JE, Allen JT, McLean BN, Brown AY, Vreken P, Waterham HR, Wanders RJ.
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| Nat Genet 24(2):188-91. 2000
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