Striking intrafamilial phenotypic variability in Aicardi–Goutières syndrome associated with the recurrent Asian founder mutation in RNASEH2C
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Y. Crow | T. Southwood | J. Vogt | L. Macpherson | C. Oley | S. Philip | S. Agrawal | M. Bhole | Zala Ibrahim | Malini V. Bhole