Cite
HARVARD Citation
Marelli, C. et al. (2016). Mini‐Exome Coupled to Read‐Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias. Human mutation. 37 (12), pp. 1340-1353. [Online].
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Marelli, C. et al. (2016). Mini‐Exome Coupled to Read‐Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias. Human mutation. 37 (12), pp. 1340-1353. [Online].