APA citiranje

Peng, G., Liu, P., He, F., & Luo, B. (2016). Posterior cortical atrophy as a primary clinical phenotype of corticobasal syndrome with a progranulin gene rs5848 TT genotype. Orphanet J Rare Dis.

Citação norma Chicago

Peng, Guoping, Ping Liu, Fangping He, and Benyan Luo. "Posterior Cortical Atrophy As a Primary Clinical Phenotype of Corticobasal Syndrome With a Progranulin Gene Rs5848 TT Genotype." Orphanet J Rare Dis 2016.

MLA citiranje

Peng, Guoping, Ping Liu, Fangping He, and Benyan Luo. "Posterior Cortical Atrophy As a Primary Clinical Phenotype of Corticobasal Syndrome With a Progranulin Gene Rs5848 TT Genotype." Orphanet J Rare Dis 2016.