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A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2. [electronic resource] by
- Chan, Barden
- Clasquin, Michelle
- Smolen, Gromoslaw A
- Histen, Gavin
- Powe, Josh
- Chen, Yue
- Lin, Zhizhong
- Lu, Chenming
- Liu, Yan
- Cang, Yong
- Yan, Zhonghua
- Xia, Yuanfeng
- Thompson, Ryan
- Singleton, Chris
- Dorsch, Marion
- Silverman, Lee
- Su, Shin-San Michael
- Freeze, Hudson H
- Jin, Shengfang
Producer: 20170925
In:
Human molecular genetics vol. 25
Availability: No items available.
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