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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: 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
Jezik:Inglês
Izdano: 1999
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377979/
https://ncbi.nlm.nih.gov/pubmed/10441579
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items