Two new mild homozygous mutations in Gaucher disease patients: clinical signs and biochemical analyses.

MLA

Cormand, B., et al. “Two New Mild Homozygous Mutations in Gaucher Disease Patients: Clinical Signs and Biochemical Analyses.” American Journal of Medical Genetics, vol. 70, no. 4, June 1997, pp. 437–43. EBSCOhost, https://doi.org/10.1002/(sici)1096-8628(19970627)70:4<437::aid-ajmg19>3.0.co;2-i.

APA

Cormand, B., Grinberg, D., Gort, L., Fiumara, A., Barone, R., Vilageliu, L., & Chabás, A. (1997). Two new mild homozygous mutations in Gaucher disease patients: clinical signs and biochemical analyses. American Journal of Medical Genetics, 70(4), 437–443. https://doi.org/10.1002/(sici)1096-8628(19970627)70:4<437::aid-ajmg19>3.0.co;2-i

Chicago

Cormand, B, D Grinberg, L Gort, A Fiumara, R Barone, L Vilageliu, and A Chabás. 1997. “Two New Mild Homozygous Mutations in Gaucher Disease Patients: Clinical Signs and Biochemical Analyses.” American Journal of Medical Genetics 70 (4): 437–43. doi:10.1002/(sici)1096-8628(19970627)70:4<437::aid-ajmg19>3.0.co;2-i.