APA

Revy P., Muto T., Levy Y., Geissmann F., Plebani A., Sanal O., Catalan N., Forveille M., Dufourcq-Labelouse R., Gennery A., Tezcan I., Ersoy F., Kayserili H., Ugazio A. G., Brousse N., Muramatsu M., Notarangelo L. D., Kinoshita K., Honjo T., Fischer A. & Durandy A. (20001004). Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2). : Cell.

Chicago

Revy P, Muto T, Levy Y, Geissmann F, Plebani A, Sanal O, Catalan N, Forveille M, Dufourcq-Labelouse R, Gennery A, Tezcan I, Ersoy F, Kayserili H, Ugazio A G, Brousse N, Muramatsu M, Notarangelo L D, Kinoshita K, Honjo T, Fischer A and Durandy A. 20001004. Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2). : Cell.

Harvard

Revy P., Muto T., Levy Y., Geissmann F., Plebani A., Sanal O., Catalan N., Forveille M., Dufourcq-Labelouse R., Gennery A., Tezcan I., Ersoy F., Kayserili H., Ugazio A. G., Brousse N., Muramatsu M., Notarangelo L. D., Kinoshita K., Honjo T., Fischer A. and Durandy A. (20001004). Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2). : Cell.

MLA

Revy P, Muto T, Levy Y, Geissmann F, Plebani A, Sanal O, Catalan N, Forveille M, Dufourcq-Labelouse R, Gennery A, Tezcan I, Ersoy F, Kayserili H, Ugazio A G, Brousse N, Muramatsu M, Notarangelo L D, Kinoshita K, Honjo T, Fischer A and Durandy A. Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2). : Cell. 20001004.