A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis.

MLA

Borthwick, K. J., et al. “A Phenocopy of CAII Deficiency: A Novel Genetic Explanation for Inherited Infantile Osteopetrosis with Distal Renal Tubular Acidosis.” Journal of Medical Genetics, vol. 40, no. 2, Feb. 2003, pp. 115–21. EBSCOhost, https://doi.org/10.1136/jmg.40.2.115.

APA

Borthwick, K. J., Kandemir, N., Topaloglu, R., Kornak, U., Bakkaloglu, A., Yordam, N., Ozen, S., Mocan, H., Shah, G. N., Sly, W. S., & Karet, F. E. (2003). A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis. Journal of Medical Genetics, 40(2), 115–121. https://doi.org/10.1136/jmg.40.2.115

Chicago

Borthwick, K. J., N. Kandemir, R. Topaloglu, U. Kornak, A. Bakkaloglu, N. Yordam, S. Ozen, et al. 2003. “A Phenocopy of CAII Deficiency: A Novel Genetic Explanation for Inherited Infantile Osteopetrosis with Distal Renal Tubular Acidosis.” Journal of Medical Genetics 40 (2): 115–21. doi:10.1136/jmg.40.2.115.