中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A novel missense mutation in the acid alpha-glucosidase gene causing the classic infantile form of Pompe disease

文献类型:期刊论文

作者Dou, W; Peng, C; Zheng, J; Gu, XF; Fu, LJ; Martiniuk, F; Sheng, HZ
刊名CLINICA CHIMICA ACTA
出版日期2006
卷号374期号:1页码:145-146
通讯作者Sheng, HZ (reprint author), Shanghai Jiao Tong Univ, Sch Med, Ctr Dev Biol, Xinhua Hosp, Shanghai 200092, Peoples R China.,hzsheng2003@yahoo.com
学科主题Medical Laboratory Technology
类目[WOS]Medical Laboratory Technology
关键词[WOS]GENOTYPE-PHENOTYPE CORRELATION
收录类别SCI
语种英语
WOS记录号WOS:000242040100021
版本出版稿
源URL[http://202.127.25.143/handle/331003/1811]  
专题上海生化细胞研究所_上海生科院生化细胞研究所
推荐引用方式
GB/T 7714
Dou, W,Peng, C,Zheng, J,et al. A novel missense mutation in the acid alpha-glucosidase gene causing the classic infantile form of Pompe disease[J]. CLINICA CHIMICA ACTA,2006,374(1):145-146.
APA Dou, W.,Peng, C.,Zheng, J.,Gu, XF.,Fu, LJ.,...&Sheng, HZ.(2006).A novel missense mutation in the acid alpha-glucosidase gene causing the classic infantile form of Pompe disease.CLINICA CHIMICA ACTA,374(1),145-146.
MLA Dou, W,et al."A novel missense mutation in the acid alpha-glucosidase gene causing the classic infantile form of Pompe disease".CLINICA CHIMICA ACTA 374.1(2006):145-146.

入库方式: OAI收割

来源:上海生物化学与细胞生物学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。