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Protein misfolding and clearance in the pathogenesis of a n..:
Martínez-Rubio, Dolores
;
Rodriguez-Prieto, Ángela
;
Sancho, Paula
...
Human Molecular Genetics;31(22). , 2022
Link:
https://hdl.handle.net/11351/8545
RT Journal T1
Protein misfolding and clearance in the pathogenesis of a new infantile onset ataxia caused by mutations in PRDX3
UL https://suche.suub.uni-bremen.de/peid=base-ftscientia:oai:scientiasalut.gencat.cat:11351_8545&Exemplar=1&LAN=DE A1 Martínez-Rubio, Dolores A1 Rodriguez-Prieto, Ángela A1 Sancho, Paula A1 Navarro-González, Carmen A1 Gorría-Redondo, Nerea A1 Miquel-Leal, Javier A1 Perez Dueñas, Belen PB Oxford University Press YR 2022 K1 Atàxia - Aspectes genètics K1 Cerebel - Degeneració K1 Pediatria K1 DISEASES::Nervous System Diseases::Neurologic Manifestations::Dyskinesias::Ataxia K1 Other subheadings::Other subheadings::Other subheadings::/genetics K1 CHEMICALS AND DRUGS::Amino Acids K1 Peptides K1 and Proteins::Proteins::Mitochondrial Proteins K1 DISEASES::Nervous System Diseases::Central Nervous System Diseases::Brain Diseases::Cerebellar Diseases::Spinocerebellar Degenerations K1 ENFERMEDADES::enfermedades del sistema nervioso::manifestaciones neurológicas::discinesias::ataxia K1 Otros calificadores::Otros calificadores::Otros calificadores::/genética K1 COMPUESTOS QUÍMICOS Y DROGAS::aminoácidos K1 péptidos y proteínas::proteínas::proteínas mitocondriales K1 ENFERMEDADES::enfermedades del sistema nervioso::enfermedades del sistema nervioso central::enfermedades cerebrales::enfermedades cerebelosas::degeneraciones espinocerebelosas JF Human Molecular Genetics;31(22) LK http://dx.doi.org/https://hdl.handle.net/11351/8545 DO https://hdl.handle.net/11351/8545 SF ELIB - SuUB Bremen
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