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Wiley, Clinical Genetics, 6(96), p. 585-589, 2019

DOI: 10.1111/cge.13632

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The activating p.Ser466Arg change in STAT1 causes a peculiar phenotype with features of interferonopathies

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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