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Brain somatic mutations in SLC35A2 cause intractable epilepsy with aberrant N-glycosylation
OBJECTIVE: To identify whether somatic mutations in SLC35A2 alter N-glycan structures in human brain tissues and cause nonlesional focal epilepsy (NLFE) or mild malformation of cortical development (mMCD). METHODS: Deep whole exome and targeted sequencing analyses were conducted for matched brain an...
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| Izdano u: | Neurol Genet |
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| Glavni autori: | , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Wolters Kluwer
2018
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6283456/ https://ncbi.nlm.nih.gov/pubmed/30584598 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000294 |
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