最前沿的研究方向是基因变量研究，Ortet解释说。
The most innovative line of research is the study of genetic variables, explains Ortet.
然而，这反映的事实是一个基因变量在39%的正常人中发现，仅25%在阅读缺失病人中发现，不同的变量在对照组中30%，阅读缺失病人中35%。
However, this reflected the fact that one gene variant was found in 39% of normal readers and only 25% of dyslexics, with a different variant being seen in 30% of controls and 35% of dyslexics.
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