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Clinical presentation, molecular analysis and follow-up of patients with mut methylmalonic acidemia in Shandong province, China.
Pediatr Neonatol. 2020 Apr;61(2):148-154. doi: 10.1016/j.pedneo.2019.07.004. Epub 2019 Aug 7.
Pediatr Neonatol. 2020.
PMID: 31466887
Free article.
Two novel mutations in the BCKDHB gene that cause maple syrup urine disease.
Han B, Han B, Guo B, Liu Y, Cao Z.
Han B, et al. Among authors: cao z.
Pediatr Neonatol. 2018 Oct;59(5):515-519. doi: 10.1016/j.pedneo.2018.01.006. Epub 2018 Jan 6.
Pediatr Neonatol. 2018.
PMID: 29366676
Free article.
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Diagnosis, treatment and follow-up of patients with tetrahydrobiopterin deficiency in Shandong province, China.
Han B, Zou H, Han B, Zhu W, Cao Z, Liu Y.
Han B, et al. Among authors: cao z.
Brain Dev. 2015 Jun;37(6):592-8. doi: 10.1016/j.braindev.2014.09.008. Epub 2014 Oct 7.
Brain Dev. 2015.
PMID: 25304915
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Clinical presentation, gene analysis and outcomes in young patients with early-treated combined methylmalonic acidemia and homocysteinemia (cblC type) in Shandong province, China.
Han B, Cao Z, Tian L, Zou H, Yang L, Zhu W, Liu Y.
Han B, et al. Among authors: cao z.
Brain Dev. 2016 May;38(5):491-7. doi: 10.1016/j.braindev.2015.10.016. Epub 2015 Nov 10.
Brain Dev. 2016.
PMID: 26563984
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