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9. [Follow up and gene mutation analysis in cases suspected as 3-methylcrotonyl-coenzyme A carboxylase deficiency by neonatal screening]. Ye J; Gong L; Han L; Qiu W; Zhang H; Gao X; Jin J; Xu H; Gu X Zhonghua Er Ke Za Zhi; 2014 Jun; 52(6):409-14. PubMed ID: 25190158 [TBL] [Abstract][Full Text] [Related]
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