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Group by: Type of Work | No Grouping Number of items: 1. Meyer, Esther and Kurian, Manju A. and Pasha, Shanaz and Trembath, Richard C. and Cole, Trevor and Maher, Eamonn R. (2010) A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorption. Molecular Genetics and Metabolism, 99 (3). p. 325. ISSN 10967192 |
