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