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A haploinsufficiency of FOXG1 identified in a boy with congenital variant of Rett syndrome

✍ Scribed by Kumakura, Akira; Takahashi, Satoru; Okajima, Kazuki; Hata, Daisuke

Book ID: 122223105
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 952 KB
Volume: 36
Category: Article
ISSN: 0387-7604
DOI: 10.1016/j.braindev.2013.09.006

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