Schrauwen, I., Helfmann, S., Inagaki, A., Predoehl, F., Tabatabaiefar, M., Picher, M., . . . Van Camp, G. (2012). A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment. Elsevier.
Stile di citazione ChicagoSchrauwen, Isabelle, et al. A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment. Elsevier, 2012.
Citazione MLASchrauwen, Isabelle, et al. A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment. Elsevier, 2012.
Attenzione: Queste citazioni potrebbero non essere precise al 100%.