Cita APA

Srikrupa, N. N., Sripriya, S., Pavithra, S., Sen, P., Gupta, R., & Mathavan, S. (2021). Whole-exome sequencing identifies two novel ALMS1 mutations in Indian patients with Leber congenital amaurosis. Hum Genome Var.

Chicago Style Citation

Srikrupa, Natarajan N., Sarangapani Sripriya, Suriyanarayanan Pavithra, Parveen Sen, Ravi Gupta, i Sinnakaruppan Mathavan. "Whole-exome Sequencing Identifies Two Novel ALMS1 Mutations in Indian Patients With Leber Congenital Amaurosis." Hum Genome Var 2021.

Cita MLA

Srikrupa, Natarajan N., et al. "Whole-exome Sequencing Identifies Two Novel ALMS1 Mutations in Indian Patients With Leber Congenital Amaurosis." Hum Genome Var 2021.