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A novel PCYT2 mutation identified in a Chinese consanguineous family with hereditary spastic paraplegia.
Journal of Genetics and Genomics ( IF 6.6 ) Pub Date : 2021-07-07 , DOI: 10.1016/j.jgg.2021.06.008 Qiao Wei 1 , Wen-Jiao Luo 1 , Hao Yu 1 , Pei-Shan Wang 1 , Hai-Lin Dong 1 , Hong-Fu Li 1 , Zhi-Ying Wu 1
更新日期：2021-07-07
Journal of Genetics and Genomics ( IF 6.6 ) Pub Date : 2021-07-07 , DOI: 10.1016/j.jgg.2021.06.008 Qiao Wei 1 , Wen-Jiao Luo 1 , Hao Yu 1 , Pei-Shan Wang 1 , Hai-Lin Dong 1 , Hong-Fu Li 1 , Zhi-Ying Wu 1
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