首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Amyloid precursor protein mutation at codon 713 (Ala-->Val) does not cause schizophrenia: non-pathogenic variant found at codon 705 (silent).
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Amyloid precursor protein mutation at codon 713 (Ala-->Val) does not cause schizophrenia: non-pathogenic variant found at codon 705 (silent).

机译:713号密码子(Ala-> Val)的淀粉样蛋白前体蛋白突变不会导致精神分裂症:在705号密码子上发现非致病性变异(沉默)。

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    摘要

    In some families with early-onset Alzheimer's disease (AD) pathogenic mutations have been found in exons 16 and 17 of the amyloid precursor protein (APP) gene. One case of schizophrenia has been described with a mutation at codon 713. We have developed a single strand conformation polymorphism (SSCP) method that detects mutations in these exons and investigated 98 AD cases and 56 elderly healthy controls. An earlier reported mutation at codon 713 in a healthy control and a previously undescribed polymorphism at codon 705 in a sporadic case of AD were found. These mutations are probably not related to disease pathogenesis.
    机译:在一些患有早发型阿尔茨海默氏病(AD)的家庭中,在淀粉样前体蛋白(APP)基因的外显子16和17中发现了致病性突变。已描述一例精神分裂症患者,其密码子第713位突变。我们开发了一种单链构象多态性(SSCP)方法,可检测这些外显子中的突变,并调查了98位AD病例和56位老年健康对照者。在一个健康的对照组中,发现了较早报道的713位密码子突变,而在偶发的AD病例中,发现了705位密码子之前未描述的多态性。这些突变可能与疾病的发病机制无关。

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