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2 Publications
2018 | Journal Article | IST-REx-ID: 691 | 
Marin Valencia I, Novarino G, Johansen A, et al. A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features. Journal of Medical Genetics. 2018;55(1):48-54. doi:10.1136/jmedgenet-2017-104627
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| PubMed | Europe PMC
1983 | Book Chapter | IST-REx-ID: 4328
Barton NH, Hewitt G. Hybrid zones as barriers to gene flow. In: Oxford G, Rollinson D, eds. Protein Polymorphism: Adaptive and Taxonomic Significance. Vol 24. Academic Press; 1983:341-359.
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