Cita APA

Law, R., Dixon-Salazar, T., Jerber, J., Cai, N., Abbasi, A., Zaki, M., . . . Gleeson, J. (2014). Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability. Am J Hum Genet.

Citación estilo Chicago

Law, Rosalind, et al. "Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability." Am J Hum Genet 2014.

Cita MLA

Law, Rosalind, et al. "Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability." Am J Hum Genet 2014.