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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1999
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377979/
https://ncbi.nlm.nih.gov/pubmed/10441579
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak