Blar i Publikasjoner fra Cristin - Sykehuset Innlandet HF på tidsskrift "Brain & development (Tokyo. 1979)"
Viser treff 1-1 av 1
-
Genetic and clinical variations in a Norwegian sample diagnosed with Rett syndrome
(Peer reviewed; Journal article, 2020)Background and purpose: Rett syndrome (RTT) is a neurodevelopmental disorder mainly caused by mutations in MECP2. The diagnostic criteria of RTT are clinical; mutations in MECP2 are neither diagnostic nor necessary, and a ...