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On the likelihood of SCN1A microdeletions or duplications in Dravet syndrome with missense mutation

✍ Scribed by Shi, Xiuyu; Wang, Jiwen; Kurahashi, Hirokazu; Ishii, Atsushi; Higurashi, Norimichi; Kaneko, Sunao; Hirose, Shinichi

Book ID: 122709969
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 96 KB
Volume: 34
Category: Article
ISSN: 0387-7604
DOI: 10.1016/j.braindev.2011.11.005

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