MECP2 mutations in Danish patients with Rett syndrome: High frequency of mutations but no consistent correlations with clinical severity or with the X chomosome inactivation pattern

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Rett syndrome, mutations, MECP2, X-inactivation
OriginalsprogEngelsk
TidsskriftEuropean Journal of Human Genetics
Vol/bind9
Udgave nummer3
Sider (fra-til)178-184
ISSN1018-4813
StatusUdgivet - 2001

ID: 145906