X-linked methyl CpG binding protein (MeCP2) gene mutations in children with Rett syndrome: Correlation with clinical severity of gastrointestinal symptoms

被引:1
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Cuffari, C
Darbari, A
Bibat, G
Naidu, S
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10.1016/S0016-5085(03)80202-0
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R57 [消化系及腹部疾病];
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页码:A41 / A41
页数:1
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