A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate.

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作者： Caixia,Xian ^[1] ; Mingwei,Zhu ^[1] ; Tianying,Nong ^[1] ; Yiqiang,Li ^[2] ; Xingmei,Xie ^[1] ; Xia,Li ^[1] ; Jiangui,Li ^[2] ; Jingchun,Li ^[2] ; Jianping,Wu ^[2] ; Weizhe,Shi ^[2] ; Ping,Wei ^[1] ; Hongwen,Xu ^[2] ; Ya-Ping,Tang ^[1]

作者单位： Guangzhou Medical University, Guangzhou Women and Children's Medical Center, Guangzhou Institute of Pediatrics, Guangzhou, Guangdong Province, P.R. China. ^[1] Guangzhou Medical University, Guangzhou Women and Children's Medical Center, Department of Pediatric Orthopedics, Guangzhou, Guangdong Province, P.R. China. ^[2]

DOI 10.1590/1678-4685-GMB-2020-0334

PMID 34042151

发布时间 2021-06-08

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Genetics and molecular biology

2021年44卷2期

e20200334页

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A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate.

Genetics and molecular biology

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Genetics and molecular biology

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A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate.

Genetics and molecular biology

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Genetics and molecular biology

相关期刊

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