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CJCP  2023, Vol. 25 Issue (4): 401-406    DOI: 10.7499/j.issn.1008-8830.2211062
RARE DISEASE RESEARCH Current Issue| Next Issue| Archive| Adv Search  | 
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
Department of Dermatology, Hunan Children's Hospital, Changsha 410007, China
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