PPP1R21 homozygous null variants associated with developmental delay, muscle weakness, distinctive facial features, and brain abnormalities

J. Suleiman, A. M. Al Hashem, B. Tabarki, K. Al-Thihli, W. Bi, A. W. El-Hattab*

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

8 Citations (Scopus)

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