A method of in vitro diagnosis for predisposition, the onset or presence of autism spectrum disorder in a person. Said method includes detecting that person the existence of a change in an intronic segment of the genome, which segment is located at least within the portion of chromosome 7 as set forth in SEQ. ID. NO: 1 and wherein said change comprises a G to A transition at position 5579 and / or a T to C transition at position 5731 of SEQ. ID. No.1.
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机译：一种对人的易感性，自闭症谱系障碍的发作或存在进行体外诊断的方法。所述方法包括检测该人基因组内含子区段中是否存在变化，该区段至少位于SEQ ID NO：1所示的7号染色体部分内。 ID。 NO：1，其中所述变化包括在SEQ.ID.No.5的位置5579处的G到A的转变和/或在位置7311的位置上的T到C的转变。 ID。 1号
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