婴儿型多羧化酶缺乏症误诊1例

Chinese Journal of Child Health Care ›› 2015, Vol. 23 ›› Issue (11) : 1231-1232.

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Chinese Journal of Child Health Care ›› 2015, Vol. 23 ›› Issue (11) : 1231-1232. DOI: 10.11852/zgetbjzz2015-23-11-36

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[1] 石超,常建民.多羧化酶缺乏症[J].临床皮肤科杂志,2007,36(11):737-738.
[2] 沈晓明,朱建幸,孙琨.尼尔森儿科学上册[M].17版.北京:北京大学医学出版社,2007,503-514.
[3] 李秀珍,刘丽,盛慧英,等.多种羧化酶缺乏症15例临床分析及长期随访[J].中华实用儿科临床杂志,2014,29(8):590-594.
[4] Hui J,Law E,Chung C,et al.The first reported HLCS gene mutation causing holocarboxylase synthetase deficiency in a Vietnamese patient[J].World J Pediatr,2012,8(3):278-280.
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