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Article

Extending the clinical phenotype associated with biallelic NTHL1 germline mutations

24 Sept 2018

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 30248171
DOI: 10.1111/cge.13444

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Extending the clinical phenotype associated with biallelic NTHL1 germline mutationsPMID 30248171Read ↗

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