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Academic Press

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Prevalence of the Methylenetetrahydrofolate Reductase (MTHFR) C677T Mutation in Patients with Varicose Veins of Lower Limbs

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Identification and Characterization of a Novel Mutation c.1090G>T (G325W) and Nine Common Mutant Alleles Leading to Gaucher Disease in Spanish Patients

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Selective IgG2 deficiency due to a point mutation causing abnormal splicing of the C2 gene

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A Novel CFTR Frame-Shift Mutation, 935delA, in Two Hispanic Cystic Fibrosis Patients

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