Mutations in exon 1 of MECP2B are not a common cause of X-linked mental 
retardation in males

Poirier, Karine; Francis, Fiona; Hamel, Ben; Moraine, Claude; Fryns, Jean Pierre; Ropers, Hans-Hilger; Chelly, Jamel; Bienvenu, Thierry

doi:10.1038/sj.ejhg.5201399

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Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males

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Ropers, Hans-Hilger
Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Poirier, K., Francis, F., Hamel, B., Moraine, C., Fryns, J. P., Ropers, H.-H., et al. (2005). Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males. Druckausgaben (und Verfilmungen), 13(5), 523-524. doi:10.1038/sj.ejhg.5201399.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-86AF-A

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