Extensive cerebral white matter abnormality without clinical symptoms: A new hereditary condition?
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
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1. A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations;European Journal of Neurology;2009-12-04
2. A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy;Journal of Neurology, Neurosurgery & Psychiatry;2009-02-01
3. Adult-onset autosomal dominant leukodystrophy with autonomic symptoms restricted to 1.5 Mbp on chromosome 5q23;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2006
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