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

✍ Scribed by Poirier, Karine; Francis, Fiona; Hamel, Ben; Moraine, Claude; Fryns, Jean Pierre; Ropers, Hans H; Chelly, Jamel; Bienvenu, Thierry

Book ID: 110026203
Publisher: Nature Publishing Group
Year: 2005
Tongue: English
Weight: 52 KB
Volume: 13
Category: Article
ISSN: 1018-4813
DOI: 10.1038/sj.ejhg.5201399

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