Cite
HARVARD Citation
Ekong, R. et al. (2016). Variants Within TSC2 Exons 25 and 31 Are Very Unlikely to Cause Clinically Diagnosable Tuberous Sclerosis. Human mutation. 37 (4), pp. 364-370. [Online].
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Ekong, R. et al. (2016). Variants Within TSC2 Exons 25 and 31 Are Very Unlikely to Cause Clinically Diagnosable Tuberous Sclerosis. Human mutation. 37 (4), pp. 364-370. [Online].