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5. Mutations of PQBP1 in Renpenning syndrome gain the function of promoting ubiquitin-mediated degradat

Mutations of PQBP1 in Renpenning syndrome gain the function of promoting ubiquitin-mediated degradat

来源 :第三届全国发育生物学大会 | 被引量 : 0次 | 上传用户：yangmingmind

【摘 要】

：

Renpenning syndrome is a group of X-linked intellectual disability (XLID) syndromes caused by mutations in human polyglutamine-binding protein 1 (PQBP1) gene.

【作 者】

：

Xiao-Yan Zhang Yu-Qian Shen Xian Liu Junhai Han Zi Chao Zhang 

【机 构】

：

Institute of Life Sciences, Southeast University, Nanjing, Jiangsu, 210096, P.R.China

【出 处】

：

第三届全国发育生物学大会

【发表日期】

：

2016年8期

【关键词】

：

X-linked intellectual disability synaptic function protein degradation PQBP1 FMR 

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　　Renpenning syndrome is a group of X-linked intellectual disability (XLID) syndromes caused by mutations in human polyglutamine-binding protein 1 (PQBP1) gene.

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