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 tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Rett syndrome, mutations, MECP2, X-inactivation
Originalsprog | Engelsk |
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Tidsskrift | European Journal of Human Genetics |
Vol/bind | 9 |
Udgave nummer | 3 |
Sider (fra-til) | 178-184 |
ISSN | 1018-4813 |
Status | Udgivet - 2001 |
ID: 145906