CNTNAP2基因与汉族儿童孤独症的病例对照研究(3)
[8] Poot M, Beyer V, Schwaab I, et al. Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder[J]. Neurogenetics,2010, 11(1):81-89.[9] Anderson G R ......
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