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HARVARD Citation
Fox, J. et al. (2017). Rare familial TSC2 gene mutation associated with atypical phenotype presentation of Tuberous Sclerosis Complex. American journal of medical genetics. 173 (3), pp. 744-748. [Online].
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Fox, J. et al. (2017). Rare familial TSC2 gene mutation associated with atypical phenotype presentation of Tuberous Sclerosis Complex. American journal of medical genetics. 173 (3), pp. 744-748. [Online].