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QDPR gene mutation and clinical follow-up in Chinese patients with dihydropteridine reductase deficiency.
World J Pediatr. 2014 Aug;10(3):219-26. doi: 10.1007/s12519-014-0496-7. Epub 2014 Aug 15.
World J Pediatr. 2014.
PMID: 25124972
Application of isoxanthopterin as a new pterin marker in the differential diagnosis of hyperphenylalaninemia.
Bao PZ, Ye J, Han LS, Qiu WJ, Zhang HW, Yu YG, Wang JG, Gu XF.
Bao PZ, et al.
World J Pediatr. 2019 Feb;15(1):66-71. doi: 10.1007/s12519-018-0202-2. Epub 2018 Nov 15.
World J Pediatr. 2019.
PMID: 30443829
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Examining the blood amino acid status in pretherapeutic patients with hyperphenylalaninemia.
Liang L, Ye J, Han L, Qiu W, Zhang H, Yu Y, Zhu T, Xu F, Zhan X, Bao P, Ji W, Gu X.
Liang L, et al.
J Clin Lab Anal. 2020 Mar;34(3):e23106. doi: 10.1002/jcla.23106. Epub 2019 Nov 24.
J Clin Lab Anal. 2020.
PMID: 31762087
Free PMC article.
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