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Fjær, R. et al. (2021). A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome. Human molecular genetics. 30 (21), pp. 1919-1931. [Online].
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Fjær, R. et al. (2021). A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome. Human molecular genetics. 30 (21), pp. 1919-1931. [Online].