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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Autores principales: 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
Formato: Artigo
Lenguaje:Inglês
Publicado: 1999
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377979/
https://ncbi.nlm.nih.gov/pubmed/10441579
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