De Siervi, A., Mendez, M., Parera, V., Varela, L., Batlle, A., & Rossetti, M. Acute intermittent porphyria: Characterization of two novel mutations in the porphobilinogen deaminase gene, one amino acid deletion (453-455delAGC) and one splicing aceptor site mutation (IVS8-1G>T).
Cita Chicago Style (17a ed.)De Siervi, A., M. Mendez, V.E Parera, L. Varela, A.M Batlle, y M.V Rossetti. Acute Intermittent Porphyria: Characterization of Two Novel Mutations in the Porphobilinogen Deaminase Gene, One Amino Acid Deletion (453-455delAGC) and One Splicing Aceptor Site Mutation (IVS8-1G>T).
Cita MLA (8a ed.)De Siervi, A., et al. Acute Intermittent Porphyria: Characterization of Two Novel Mutations in the Porphobilinogen Deaminase Gene, One Amino Acid Deletion (453-455delAGC) and One Splicing Aceptor Site Mutation (IVS8-1G>T).