The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27.

Leukoencephalopathy with vanishing white matter (VWM) is an autosomal recessive disorder with normal early development and, usually, childhood-onset neurological deterioration. At present, diagnosis of VWM is based on clinical examination and the results of repeat magnetic resonance imaging and magn...

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Bibliographic Details
Main Authors: Leegwater, P A, Könst, A A, Kuyt, B, Sandkuijl, L A, Naidu, S, Oudejans, C B, Schutgens, R B, Pronk, J C, van der Knaap, M S
Format: Artigo
Language:Inglês
Published: 1999
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377979/
https://ncbi.nlm.nih.gov/pubmed/10441579
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