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Li, L. et al. (2015). A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype. Journal of medical genetics. 52 (5), pp. 348-352. [Online].
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Li, L. et al. (2015). A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype. Journal of medical genetics. 52 (5), pp. 348-352. [Online].