(Q41931274)
Statements
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A haploinsufficiency of FOXG1 identified in a boy with congenital variant of Rett syndrome (English)
1 reference
Akira Kumakura
1 reference
Satoru Takahashi
1 reference
Kazuki Okajima
1 reference
Daisuke Hata
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16 October 2013
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36
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8
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725-729
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Identifiers
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1 reference