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1 Ergebnisse
1
Modeling Rare Human Disorders in Mice : The Finnish Disease..:
Zárybnický, Tomáš
;
Heikkinen, Anne
;
Kangas, Salla M
...
10.3390/cells10113158. , 2022
Link:
http://hdl.handle.net/10138/338820
RT Journal T1
Modeling Rare Human Disorders in Mice : The Finnish Disease Heritage
UL https://suche.suub.uni-bremen.de/peid=base-ftunivhelsihelda:oai:helda.helsinki.fi:10138_338820&Exemplar=1&LAN=DE A1 Zárybnický, Tomáš A1 Heikkinen, Anne A1 Kangas, Salla M A1 Karikoski, Marika A1 Martinez-Nieto, Guillermo Antonio A1 Salo, Miia H A1 Uusimaa, Johanna A1 Vuolteenaho, Reetta A1 Hinttala, Reetta A1 Sipilä, Petra A1 Kuure, Satu PB MDPI YR 2022 K1 rare diseases K1 monogenic diseases K1 mouse models K1 CRISPR/Cas9 K1 genome engineering K1 Finnish disease heritage K1 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY K1 NEURONAL CEROID-LIPOFUSCINOSIS K1 LYSOSOMAL STORAGE DISORDER K1 CARTILAGE-HAIR HYPOPLASIA K1 MITOCHONDRIAL TRIFUNCTIONAL PROTEIN K1 STEM-CELL TRANSPLANTATION K1 DEGENERATION MND MUTANT K1 ACUTE FATTY LIVER K1 MOUSE MODEL K1 HYDROLETHALUS SYNDROME K1 Biochemistry K1 cell and molecular biology JF 10.3390/cells10113158 LK http://hdl.handle.net/10138/338820 DO http://hdl.handle.net/10138/338820 SF ELIB - SuUB Bremen
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