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Prevalence of common mutations in the arylsulphatase A gene in metachromatic leukodystrophy patients diagnosed in Britain

Mendelian DisorderAutoimmune DiseaseArylsulphatase A GeneGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyHematologyPathologyCommon MutationsDisease Gene IdentificationMedicineMetachromatic Leukodystrophy PatientsClinical Genetics