| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10833045 | Molecular Genetics and Metabolism | 2015 | 6 Pages |
Abstract
A case definition of leukodystrophies and classification of heritable white matter disorders will permit more detailed epidemiologic studies of these disorders.
Keywords
CADASILAxDMCT8GM2 gangliosidosisMLCX-linked adrenoleukodystrophyGLENCLClC-2X-ALDGM1GM2AGSMSUD4H syndromeGM1 gangliosidosisNaAmegalencephalic leukoencephalopathy with subcortical cystsneuronal ceroid lipofuscinosisN-Acetyl-AspartateMRIIEMMaple syrup urine diseasealexander diseaseMagnetic resonance imagingMonocarboxylate transporter 8Inborn errors of metabolismCNScentral nervous systemLeukodystrophyMyelinGlia
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Authors
Adeline Vanderver, Morgan Prust, Davide Tonduti, Fanny Mochel, Heather M. Hussey, Guy Helman, James Garbern, Florian Eichler, Pierre Labauge, Patrick Aubourg, Diana Rodriguez, Marc C. Patterson, Johan L.K. Van Hove, Johanna Schmidt, Nicole I. Wolf,