Associated Papers
Primer on genes encoding enzymes in sialic acid metabolism in mammals.
Wickramasinghe S et al.
Biochimie, 2011
Molecular and cellular basis of lysosomal transmembrane protein dysfunction.
Ruivo R et al.
Biochimica Et Biophysica Acta, 2009
Molecular pathogenesis of sialic acid storage diseases: insight gained from four missense mutations and a putative polymorphism of human sialin.
Ruivo R et al.
Biology of the Cell, 2008
Clinical, morphological, and molecular aspects of sialic acid storage disease manifesting in utero.
Froissart R et al.
Journal of Medical Genetics, 2005
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