Delfau, M. H., Picat, C., de Rooij, F. W., Hamer, K., Bogard, M., Wilson, J. H., . . . Grandchamp, B. (1990). Two different point G to A mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyria.

Delfau, M H., C. Picat, F W. de Rooij, K. Hamer, M. Bogard, J H. Wilson, J C. Deybach, Y. Nordmann, and B. Grandchamp. Two Different Point G to A Mutations in Exon 10 of the Porphobilinogen Deaminase Gene Are Responsible for Acute Intermittent Porphyria. 1990.

Delfau, M H., et al. Two Different Point G to A Mutations in Exon 10 of the Porphobilinogen Deaminase Gene Are Responsible for Acute Intermittent Porphyria. 1990.