The Gene for Leukoencephalopathy with Vanishing White Matter Is Located on Chromosome 3q27
- 1 September 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (3), 728-734
- https://doi.org/10.1086/302548
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- Proton magnetic resonance spectroscopic imaging in childhood ataxia with diffuse central nervous system hypomyelinationNeurology, 1995
- A method for constructing radiation hybrid maps of whole genomesNature Genetics, 1994
- Childhood ataxia with diffuse central nervous system hypomyelinationAnnals of Neurology, 1994
- A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsiesNature Genetics, 1994
- Dejerine–Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) geneNature Genetics, 1993
- Diffuse White Matter Disease in Three Children: An Encephalopathy with Unique Features on Magnetic Resonance Imaging and Proton Magnetic Resonance SpectroscopyNeuropediatrics, 1993
- Evidence for a recessive PMP22 point mutation in Charcot–Marie–Tooth disease type 1ANature Genetics, 1993
- A bifunctional protein with deficient enzymic activity: Identification of a new peroxisomal disorder using novel methods to measure the peroxisomal β‐oxidation enzyme activitiesJournal of Inherited Metabolic Disease, 1990
- Peroxisomal bifunctional enzyme deficiency.Journal of Clinical Investigation, 1989