APA (7th ed.) Citation

Darvish, H., Azcona, L. J., Tafakhori, A., Ahmadi, M., Ahmadifard, A., & Paisán-Ruiz, C. (2017). Whole genome sequencing identifies a novel homozygous exon deletion in the NT5C2 gene in a family with intellectual disability and spastic paraplegia. NPJ genomic medicine, 2(1), N.PAG. https://doi.org/10.1038/s41525-017-0022-7

Chicago Style (17th ed.) Citation

Darvish, Hossein, Luis J. Azcona, Abbas Tafakhori, Mona Ahmadi, Azadeh Ahmadifard, and Coro Paisán-Ruiz. "Whole Genome Sequencing Identifies a Novel Homozygous Exon Deletion in the NT5C2 Gene in a Family with Intellectual Disability and Spastic Paraplegia." NPJ Genomic Medicine 2, no. 1 (2017): N.PAG. https://doi.org/10.1038/s41525-017-0022-7.

MLA (9th ed.) Citation

Darvish, Hossein, et al. "Whole Genome Sequencing Identifies a Novel Homozygous Exon Deletion in the NT5C2 Gene in a Family with Intellectual Disability and Spastic Paraplegia." NPJ Genomic Medicine, vol. 2, no. 1, 2017, p. N.PAG, https://doi.org/10.1038/s41525-017-0022-7.