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

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Published in Eur J Hum Genet on March 01, 2001

Authors

J B Nielsen1, K F Henriksen, C Hansen, A Silahtaroglu, M Schwartz, N Tommerup

Author Affiliations

1: Department of Clinical Genetics, Rigshospitalet University Hospital, University of Copenhagen, Blegdamsvej 9, DK-2100 Copenhagen Ø, Denmark. bieber@rh.dk

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