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1 Ergebnisse
1
Abnormal creatine transport of mutations in monocarboxylate..:
Stäubli, Andrina
;
Capatina, Nadejda
;
Fuhrer, Yvonne
...
info:eu-repo/semantics/altIdentifier/doi/10.1093/hmg/ddx310. , 2017
Link:
https://hdl.handle.net/20.500.11850/220125
RT Journal T1
Abnormal creatine transport of mutations in monocarboxylate transporter 12 (MCT12) found in patients with age-related cataract can be partially rescued by exogenous chaperone CD147
UL https://suche.suub.uni-bremen.de/peid=base-ftethz:oai:www.research-collection.ethz.ch:20.500.11850_220125&Exemplar=1&LAN=DE A1 Stäubli, Andrina A1 Capatina, Nadejda A1 Fuhrer, Yvonne A1 Munier, Francis L A1 Labs, Stephan A1 Schorderet, Daniel F A1 Tiwari, Amit A1 Verrey, Francois A1 Heon, Elise A1 Cheng, Ching-Yu A1 Wong, Tien-Yin A1 Berger, Wolfgang A1 Camargo, Simone M.R A1 Kloeckener-Gruissem, Barbara PB Oxford University Press YR 2017 K1 mutation K1 amino acids K1 cataract K1 ethnic group K1 exons K1 genes K1 lens K1 crystalline K1 membrane transport proteins K1 tissue membrane K1 molecular chaperones K1 monocarboxylic acid transporters K1 nucleotides K1 oocytes K1 single nucleotide polymorphism K1 xenopus laevis K1 creatine K1 senile K1 asian JF info:eu-repo/semantics/altIdentifier/doi/10.1093/hmg/ddx310 LK http://dx.doi.org/https://hdl.handle.net/20.500.11850/220125 DO https://hdl.handle.net/20.500.11850/220125 SF ELIB - SuUB Bremen
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