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Dive into the research topics of 'Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations'. Together they form a unique fingerprint.- Sort by
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Kirstine Ravn, Gitte Roende, Morten Duno, Kathrine Fuglsang, Kristin L Eiklid, Zeynep Tümer, Jytte B Nielsen, Ola H Skjeldal