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Clinical and biochemical abnormalities in a patient with dihydropyrimidine dehydrogenase deficiency due to homozygosity for the C29R mutation

✍ Scribed by A. B. P. Van Kuilenburg; P. Vreken; D. Riva; G. Botteon; N. G. G. M. Abeling; H. D. Bakker; A. H. Van Gennip

Book ID: 110225064
Publisher: Springer
Year: 1999
Tongue: English
Weight: 32 KB
Volume: 22
Category: Article
ISSN: 0141-8955
DOI: 10.1023/a:1005470524203

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