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Prognostic values of soluble CD30 and CD30 gene polymorphisms in heart transplantation
UploadMyelin-Associated Glycoprotein is Altered in a Familial Late-Onset Orthochromatic Leukodystrophy
Download from doi.orgFMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia
Download from www.researchgate.netSix novel ATM mutations in Italian patients with classical ataxia-telangiectasia.
Download from www.researchgate.netCOL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome
Download from www.researchgate.netDefective function of Fas in patients with type 1 diabetes associated with other autoimmune diseases
Download from journals.orgA recurrent breakpoint in the most common deletion of the Ig heavy chain locus (del A1-GP-G2-G4-E)
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