Cita APA

Cao, L., Peng, C., Yu, J., Jiang, W., & Yang, J. (2020). Identification of two novel PRPF31 mutations in Chinese families with non‐syndromic autosomal dominant retinitis pigmentosa. Mol Genet Genomic Med.

Citación estilo Chicago

Cao, Li, Chunyan Peng, Jing Yu, Wei Jiang, y Jiyun Yang. "Identification of Two Novel PRPF31 Mutations in Chinese Families With Non‐syndromic Autosomal Dominant Retinitis Pigmentosa." Mol Genet Genomic Med 2020.

Cita MLA

Cao, Li, et al. "Identification of Two Novel PRPF31 Mutations in Chinese Families With Non‐syndromic Autosomal Dominant Retinitis Pigmentosa." Mol Genet Genomic Med 2020.