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Academic Press

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X-linked severe combined immunodeficiency: from molecular cause to gene therapy within seven years

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Development of Autologous T Lymphocytes in Two Males with X-Linked Severe Combined Immune Deficiency: Molecular and Cellular Characterization

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A Novel Aminoterminal Mutation in the KAL-1 Gene in a Large Pedigree with X-Linked Kallmann Syndrome

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