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2018 | Journal Article | IST-REx-ID: 691 |
I. Marin Valencia et al., “A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features,” Journal of Medical Genetics, vol. 55, no. 1. BMJ Publishing Group, pp. 48–54, 2018.View | DOI | Download Submitted Version (ext.) | WoS | PubMed | Europe PMC
2018 | Journal Article | IST-REx-ID: 410 |
J. Masís, D. Mankus, S. Wolff, G. Guitchounts, M. A. Jösch, and D. Cox, “A micro-CT-based method for quantitative brain lesion characterization and electrode localization,” Scientific Reports, vol. 8, no. 1. Nature Publishing Group, 2018.View | Files available | DOI | WoS