A novel CPT1C variant causes pure hereditary spastic paraplegia with benign clinical course
A novel CPT1C variant causes pure hereditary spastic paraplegia with benign clinical course
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DOI:
10.1002/acn3.717
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发表时间:
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期刊:
影响因子:
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通讯作者:
Zhang J
中科院分区:
文献类型:
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作者:
Hong D;Cong L;Zhong S;Liu L;Xu Y;Zhang J