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HARVARD Citation
Owen, C. et al. (2018). Extending the phenotype associated with the CSNK2A1‐related Okur–Chung syndrome—A clinical study of 11 individuals. American journal of medical genetics. 176 (5), pp. 1108-1114. [Online].
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Owen, C. et al. (2018). Extending the phenotype associated with the CSNK2A1‐related Okur–Chung syndrome—A clinical study of 11 individuals. American journal of medical genetics. 176 (5), pp. 1108-1114. [Online].