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Identification of the first deep intronic mutation in the RPS6KA3 gene in a patient with a severe form of Coffin–Lowry syndrome

✍ Scribed by Schneider, Anne; Maas, Saskia M.; Hennekam, Raoul C.M.; Hanauer, André

Book ID: 120016825
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 636 KB
Volume: 56
Category: Article
ISSN: 1769-7212
DOI: 10.1016/j.ejmg.2012.11.007

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