De Siervi, A., Mendez, M., Parera, V. E., Batlle, A. M. d. C., & Rossetti, M. V. (1999). 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, Adriana, Manuel Mendez, Victoria Estela Parera, Alcira María del Carmen Batlle, y María Victoria 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). 1999.
Cita MLA (8a ed.)De Siervi, Adriana, 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). 1999.