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Characterization of a disease-causing Lys329 to Glu mutation in 16 patients with medium-chain acyl-CoA dehydrogenase deficiency. [electronic resource] by
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Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli. [electronic resource] by
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The molecular basis of canavan (aspartoacylase deficiency) disease in European non-Jewish patients. [electronic resource] by
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American journal of human genetics vol. 57
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CEREBRAL APOPLEXY. A CLINICAL, RADIOLOGICAL, ELECTROENCEPHALOGRAPHIC AND PATHOLOGICAL STUDY WITH SPECIAL REFERENCE TO THE PROGNOSIS OF CEREBRAL INFARCTION AND THE RESULT OF LONG-TERM ANTICOAGULATION THERAPY. [electronic resource] by
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Moclobemide in depression: a randomized, multicentre trial against isocarboxazide and clomipramine emphasizing atypical depression. [electronic resource] by
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Effect of 'attenuated' mutations in mucopolysaccharidosis IVA on molecular phenotypes of N-acetylgalactosamine-6-sulfate sulfatase. [electronic resource] by
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Normal blood pressure and plasma renin activity in mice lacking the renin-binding protein, a cellular renin inhibitor. [electronic resource] by
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Cubilin- and megalin-mediated uptake of albumin in cultured proximal tubule cells of opossum kidney. [electronic resource] by
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