Cita APA

Abhyankar, A., Lamendola‐Essel, M., Brennan, K., Giordano, J. L., Esteves, C., Felice, V., . . . Jobanputra, V. (2017). Clinical whole exome sequencing from dried blood spot identifies novel genetic defect underlying asparagine synthetase deficiency. Clin Case Rep.

Chicago Style Citation

Abhyankar, Avinash, Michelle Lamendola‐Essel, Kelly Brennan, Jessica L. Giordano, Cecilia Esteves, Vanessa Felice, Ronald Wapner, i Vaidehi Jobanputra. "Clinical Whole Exome Sequencing From Dried Blood Spot Identifies Novel Genetic Defect Underlying Asparagine Synthetase Deficiency." Clin Case Rep 2017.

Cita MLA

Abhyankar, Avinash, et al. "Clinical Whole Exome Sequencing From Dried Blood Spot Identifies Novel Genetic Defect Underlying Asparagine Synthetase Deficiency." Clin Case Rep 2017.