Cite
HARVARD Citation
Triono, A. et al. (2022). The role of whole exome sequencing in the UBE3A point mutation of Angelman Syndrome: A case report. Annals of medicine and surgery. p. . [Online].
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Triono, A. et al. (2022). The role of whole exome sequencing in the UBE3A point mutation of Angelman Syndrome: A case report. Annals of medicine and surgery. p. . [Online].