Cite
HARVARD Citation
Bossuyt, S. et al. (2021). Loss of nuclear UBE3A activity is the predominant cause of Angelman syndrome in individuals carrying UBE3A missense mutations. Human molecular genetics. 30 (6), pp. 430-442. [Online].
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Bossuyt, S. et al. (2021). Loss of nuclear UBE3A activity is the predominant cause of Angelman syndrome in individuals carrying UBE3A missense mutations. Human molecular genetics. 30 (6), pp. 430-442. [Online].