Associated Papers
Diagnosis, treatment, and follow-up of a case of Wolman disease with hemophagocytic lymphohistiocytosis.
Baronio F et al.
Molecular Genetics and Metabolism Reports, 2022
Four novel mutations identified in Norwegian patients result in intermittent maple syrup urine disease when combined with the R301C mutation.
Brodtkorb E et al.
Molecular Genetics and Metabolism, 2010
Genotype at the sIL-6R A358C polymorphism does not influence response to anti-TNF therapy in patients with rheumatoid arthritis.
Hassan B et al.
Rheumatology (oxford, England), 2010
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