Cita APA

D, N. B., JA, J., A, Y., IT, Z., A, M., SP, D., . . . F, M. (2022). Recessive variants in COL25A1 gene as novel cause of arthrogryposis multiplex congenita with ocular congenital cranial dysinnervation disorder.

Citación estilo Chicago

D, Natera-de Benito, et al. Recessive Variants in COL25A1 Gene As Novel Cause of Arthrogryposis Multiplex Congenita With Ocular Congenital Cranial Dysinnervation Disorder. 2022.

Cita MLA

D, Natera-de Benito, et al. Recessive Variants in COL25A1 Gene As Novel Cause of Arthrogryposis Multiplex Congenita With Ocular Congenital Cranial Dysinnervation Disorder. 2022.