Cita APA

Chen, W., Kahrizi, K., Meyer, N., Riazalhosseini, Y., Van Camp, G., Najmabadi, H., & Smith, R. (2005). Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus. BMJ Group.

Citación estilo Chicago

Chen, W., K. Kahrizi, N. Meyer, Y. Riazalhosseini, G. Van Camp, H. Najmabadi, y R. Smith. Mutation of COL11A2 Causes Autosomal Recessive Non-syndromic Hearing Loss At the DFNB53 Locus. BMJ Group, 2005.

Cita MLA

Chen, W., et al. Mutation of COL11A2 Causes Autosomal Recessive Non-syndromic Hearing Loss At the DFNB53 Locus. BMJ Group, 2005.