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HARVARD Citation
Suleiman, J. et al. (2018). PPP1R21 homozygous null variants associated with developmental delay, muscle weakness, distinctive facial features, and brain abnormalities. Clinical genetics. 94 (3), pp. 351-355. [Online].
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Suleiman, J. et al. (2018). PPP1R21 homozygous null variants associated with developmental delay, muscle weakness, distinctive facial features, and brain abnormalities. Clinical genetics. 94 (3), pp. 351-355. [Online].