Al-deri, N., Okur, V., Ahimaz, P., Milev, M., Valivullah, Z., Hagen, J., Sheng, Y., Chung, W., Sacher, M., & Ganapathi, M. (2020). A novel homozygous variant in TRAPPC2L results in a neurodevelopmental disorder and disrupts TRAPP complex function. Journal of Medical Genetics, 58(9), 592–601. https://doi.org/10.1136/jmedgenet-2020-107016
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Article
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10.1136/jmedgenet-2020-107016
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Scopus
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