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HARVARD Citation
Qaiser, F. et al. (2021). Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox–Gastaut syndrome. Brain communications. 3 (3), p. . [Online].
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Qaiser, F. et al. (2021). Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox–Gastaut syndrome. Brain communications. 3 (3), p. . [Online].