Raquel Ruivo
www.ciimar.up.pt
0000-0003-2412-8730
Universidade de Coimbra
23 papers found
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Molecular and cellular basis of lysosomal transmembrane protein dysfunction
Molecular pathogenesis of sialic acid storage diseases: insight gained from four missense mutations and a putative polymorphism of human sialin
The Transporters GlyT2 and VIAAT Cooperate to Determine the Vesicular Glycinergic Phenotype
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