Cite
HARVARD Citation
Baschal, E. et al. (2015). Exome Sequencing Identifies a Rare HSPG2 Variant Associated with Familial Idiopathic Scoliosis. G3. 5 (2), pp. 167-174. [Online].
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Baschal, E. et al. (2015). Exome Sequencing Identifies a Rare HSPG2 Variant Associated with Familial Idiopathic Scoliosis. G3. 5 (2), pp. 167-174. [Online].