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Fostira, F. et al. (2018). Extending the clinical phenotype associated with biallelic NTHL1 germline mutations. Clinical genetics. 94 (6), pp. 588-589. [Online].
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Fostira, F. et al. (2018). Extending the clinical phenotype associated with biallelic NTHL1 germline mutations. Clinical genetics. 94 (6), pp. 588-589. [Online].