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Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases
- Correspondence to: P Landrieu Service de Neurologie Pédiatrique, CHU Bicêtre, 94275 Le Kremlin-Bicetre Cedex, France; pierre.landrieubct.ap-hop-paris.fr
Citation
Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases
Publication history
- Received November 14, 2003
- Accepted November 17, 2003
- First published June 1, 2004.
Online issue publication
April 27, 2016
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Copyright 2004 Journal of Medical Genetics