APA (7th ed.) Citation

Bhavya Patel, Shwetal Bhatt, & Vaishali Chanpura. (2023). Rare Coexistence of SLC6A9 and TOR1A Gene Mutations in a Neonate Presenting with Hereditary Hyperekplexia and Arthrogryposis Multiplex Congenita: A Case Report with Review of Literature. Wolters Kluwer Medknow Publications.

Chicago Style (17th ed.) Citation

Bhavya Patel, Shwetal Bhatt, and Vaishali Chanpura. Rare Coexistence of SLC6A9 and TOR1A Gene Mutations in a Neonate Presenting with Hereditary Hyperekplexia and Arthrogryposis Multiplex Congenita: A Case Report with Review of Literature. Wolters Kluwer Medknow Publications, 2023.

MLA (9th ed.) Citation

Bhavya Patel, et al. Rare Coexistence of SLC6A9 and TOR1A Gene Mutations in a Neonate Presenting with Hereditary Hyperekplexia and Arthrogryposis Multiplex Congenita: A Case Report with Review of Literature. Wolters Kluwer Medknow Publications, 2023.