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Polymorphisms in DCDC2 and S100B associate with developmental dyslexia
Genetic studies of complex traits have become increasingly successful as progress is made in next-generation sequencing. We aimed at discovering single nucleotide variation present in known and new candidate genes for developmental dyslexia: CYP19A1, DCDC2, DIP2A, DYX1C1, GCFC2 (also known as C2orf3...
שמור ב:
| הוצא לאור ב: | J Hum Genet |
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| Main Authors: | , , , , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Nature Publishing Group
2015
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4521290/ https://ncbi.nlm.nih.gov/pubmed/25877001 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jhg.2015.37 |
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