APA (7th ed.) Citation

Yan Zhang, Yi Zhang, Victor Wei Zhang, Chunyi Zhang, Hongke Ding, & Aihua Yin. (2019). Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness - a case report for dual diagnosis. BMC.

Chicago Style (17th ed.) Citation

Yan Zhang, Yi Zhang, Victor Wei Zhang, Chunyi Zhang, Hongke Ding, and Aihua Yin. Mutations in Both SAMD9 and SLC19A2 Genes Caused Complex Phenotypes Characterized by Recurrent Infection, Dysphagia and Profound Deafness - a Case Report for Dual Diagnosis. BMC, 2019.

MLA (9th ed.) Citation

Yan Zhang, et al. Mutations in Both SAMD9 and SLC19A2 Genes Caused Complex Phenotypes Characterized by Recurrent Infection, Dysphagia and Profound Deafness - a Case Report for Dual Diagnosis. BMC, 2019.