Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures

Overview of attention for article published in Nature Communications, September 2015

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So far, Altmetric has seen 4 posts from 4 blogs.

New mechanism discovered behind infant epilepsyScientists at Karolinska Institutet and Karolinska University Hospital in Sweden…

Mutationen im Protein KCC2 codierenden Gen SLC12A5 können laut schwedischen Forschern zu einer schweren Form der frühkindlichen…

Scientists at Karolinska Institutet and Karolinska University Hospital in Sweden have discovered a new explanation for severe…

Researchers discover a new mechanism that appears to be responsible for infant epilepsy.

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