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The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects

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Published in 2017 at "Journal of Human Genetics"

DOI: 10.1038/jhg.2017.80

Abstract: Developmental dyslexia (DD) is a complex heritable condition characterized by impaired reading abilities. Two well-replicated candidate risk factors are as follows: (1) regulatory element associated with dyslexia 1 (READ1), which is located in intron 2… read more here.

Keywords: developmental dyslexia; risk; kiaa0319 risk; read1 kiaa0319 ... See more keywords