APA (7th ed.) Citation

Rehman, N., Ali, Z. H., Nasir, M., & Kirmani, S. Rare homozygous CNPY3 variant causing autosomal recessive developmental and epileptic encephalopathy 60: A case report. Elsevier.

Chicago Style (17th ed.) Citation

Rehman, Nohela, Zohra Hasan Ali, Mahrukh Nasir, and Salman Kirmani. Rare Homozygous CNPY3 Variant Causing Autosomal Recessive Developmental and Epileptic Encephalopathy 60: A Case Report. Elsevier.

MLA (9th ed.) Citation

Rehman, Nohela, et al. Rare Homozygous CNPY3 Variant Causing Autosomal Recessive Developmental and Epileptic Encephalopathy 60: A Case Report. Elsevier.