Liao, J., Coffman, K. A., Locker, J., Padiath, Q. S., Nmezi, B., Filipink, R. A., . . . Surti, U. (2021). Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea. Mol Genet Genomic Med.
Citación estilo ChicagoLiao, Jun, et al. "Deletion of Conserved Non‐coding Sequences Downstream From NKX2‐1: A Novel Disease‐causing Mechanism for Benign Hereditary Chorea." Mol Genet Genomic Med 2021.
Cita MLALiao, Jun, et al. "Deletion of Conserved Non‐coding Sequences Downstream From NKX2‐1: A Novel Disease‐causing Mechanism for Benign Hereditary Chorea." Mol Genet Genomic Med 2021.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.