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1 Ergebnisse
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A mouse model of a human congenital disorder of glycosylati..:
Chan, Barden
;
Clasquin, Michelle
;
Smolen, Gromoslaw A.
...
Human Molecular Genetics. 25 (2016) 11 - p. 2182-2193 , 2016
Link:
https://doi.org/10.1093/hmg/ddw085
RT Journal T1
A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddw085&Exemplar=1&LAN=DE A1 Chan, Barden A1 Clasquin, Michelle A1 Smolen, Gromoslaw A. A1 Histen, Gavin A1 Powe, Josh A1 Chen, Yue A1 Lin, Zhizhong A1 Lu, Chenming A1 Liu, Yan A1 Cang, Yong A1 Yan, Zhonghua A1 Xia, Yuanfeng A1 Thompson, Ryan A1 Singleton, Chris A1 Dorsch, Marion A1 Silverman, Lee A1 Su, Shin-San Michael A1 Freeze, Hudson H. A1 Jin, Shengfang PB Oxford University Press (OUP) YR 2016 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics VO 25 IS 11 SP 2182 OP 2193 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddw085 DO https://doi.org/10.1093/hmg/ddw085 SF ELIB - SuUB Bremen
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