A functional assay to study the pathogenicity of CHD7 protein variants encountered in CHARGE syndrome patients.

MLA

Brajadenta, Gara Samara, et al. “A Functional Assay to Study the Pathogenicity of CHD7 Protein Variants Encountered in CHARGE Syndrome Patients.” European Journal of Human Genetics : EJHG, vol. 27, no. 11, Nov. 2019, pp. 1683–91. EBSCOhost, https://doi.org/10.1038/s41431-019-0465-7.

APA

Brajadenta, G. S., Bilan, F., Gilbert-Dussardier, B., Kitzis, A., & Thoreau, V. (2019). A functional assay to study the pathogenicity of CHD7 protein variants encountered in CHARGE syndrome patients. European Journal of Human Genetics : EJHG, 27(11), 1683–1691. https://doi.org/10.1038/s41431-019-0465-7

Chicago

Brajadenta, Gara Samara, Frédéric Bilan, Brigitte Gilbert-Dussardier, Alain Kitzis, and Vincent Thoreau. 2019. “A Functional Assay to Study the Pathogenicity of CHD7 Protein Variants Encountered in CHARGE Syndrome Patients.” European Journal of Human Genetics : EJHG 27 (11): 1683–91. doi:10.1038/s41431-019-0465-7.