Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease.

MLA

Doray, B., et al. “Mutation of the RET Ligand, Neurturin, Supports Multigenic Inheritance in Hirschsprung Disease.” Human Molecular Genetics, vol. 7, no. 9, Sept. 1998, pp. 1449–52. EBSCOhost, https://doi.org/10.1093/hmg/7.9.1449.

APA

Doray, B., Salomon, R., Amiel, J., Pelet, A., Touraine, R., Billaud, M., Attié, T., Bachy, B., Munnich, A., & Lyonnet, S. (1998). Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease. Human Molecular Genetics, 7(9), 1449–1452. https://doi.org/10.1093/hmg/7.9.1449

Chicago

Doray, B, R Salomon, J Amiel, A Pelet, R Touraine, M Billaud, T Attié, B Bachy, A Munnich, and S Lyonnet. 1998. “Mutation of the RET Ligand, Neurturin, Supports Multigenic Inheritance in Hirschsprung Disease.” Human Molecular Genetics 7 (9): 1449–52. doi:10.1093/hmg/7.9.1449.