The A140V mutation in the MECP2 gene is not a common etiological factor among Brazilian mentally retarded males.

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作者： Jussara Mendonça,dos Santos ^[1] ; Cláudia Bueno,Abdalla ; Mário,Campos ; Cíntia Barros,Santos-Rebouças ; Márcia Mattos Gonçalves,Pimentel

作者单位： Departamento de Biologia Celular e Genética, Instituto de Biologia Roberto Alcântara Gomes, Universidade do Estado do Rio de Janeiro, Rua São Francisco Xavier, 524 PHLC, sala 218, Rio de Janeiro RJ 20550-013, Brazil. ^[1]

主题词青少年(Adolescent);丙氨酸(Alanine);巴西(Brazil);儿童(Child);儿童, 学龄前(Child, Preschool);DNA突变分析(DNA Mutational Analysis);DNA结合蛋白质类(DNA-Binding Proteins);疾病遗传易感性(Genetic Predisposition to Disease);人类(Humans);男(雄)性(Male);突变(Mutation);缬氨酸(Valine)

DOI 10.1016/j.neulet.2004.12.036

PMID 15814190

发布时间 2013-11-21

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Neuroscience letters

2005年379卷1期

13-6页

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The A140V mutation in the MECP2 gene is not a common etiological factor among Brazilian mentally retarded males.

Neuroscience letters

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Neuroscience letters

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The A140V mutation in the MECP2 gene is not a common etiological factor among Brazilian mentally retarded males.

Neuroscience letters

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Neuroscience letters

相关期刊

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