Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1
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| Description | scientific article published on 23 October 2018 |
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author: Rutger J Meinsma André B P van Kuilenburg Rafael Artuch Raoul Hennekam |
| Publication date | October 23, 2018 |
| Language | English |
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