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A microRNA‐328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy
OBJECTIVE: Rolandic epilepsy is a common genetic focal epilepsy of childhood characterized by centrotemporal sharp waves on electroencephalogram. In previous genome‐wide analysis, we had reported linkage of centrotemporal sharp waves to chromosome 11p13, and fine mapping with 44 SNPs identified the...
Tallennettuna:
| Julkaisussa: | Ann Clin Transl Neurol |
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| Päätekijät: | , , , , , , , , , , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
John Wiley and Sons Inc.
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4931716/ https://ncbi.nlm.nih.gov/pubmed/27386500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.320 |
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