罕见病研究：HLCS基因突变致全羧化酶合成酶缺乏症
李珂瑶, 汤建萍, 蒋艳玲, 岳淑珍, 周斌, 文容, 周泽韬, 韦祝
Holocarboxylase synthetase deficiency induced by HLCS gene mutations: a rare disease study
LI Ke-Yao, TANG Jian-Ping, JIANG Yan-Ling, YUE Shu-Zhen, ZHOU Bin, WEN Rong, HOU Ze-Tao, WEI Zhu
中国当代儿科杂志
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2023, (4): 401
-406
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DOI: 10.7499/j.issn.1008-8830.2211062
