APA (7th ed.) Citation

Mahato, S., Maddileti, S., Agrawal, T., Acharya, S., Kannabiran, C., Jalali, S., . . . Mariappan, I. Generation and validation of a Leber Congenital Amaurosis, Type 12 patient-specific iPSC line (LVPEIi006-B) with a splice-site mutation in RD3 and an isogenic mutation-corrected iPSC line (LVPEIi006-B-1). Elsevier.

Chicago Style (17th ed.) Citation

Mahato, Sudipta, Savitri Maddileti, Trupti Agrawal, Sundaram Acharya, Chitra Kannabiran, Subhadra Jalali, Debojyoti Chakraborty, and Indumathi Mariappan. Generation and Validation of a Leber Congenital Amaurosis, Type 12 Patient-specific IPSC Line (LVPEIi006-B) with a Splice-site Mutation in RD3 and an Isogenic Mutation-corrected IPSC Line (LVPEIi006-B-1). Elsevier.

MLA (9th ed.) Citation

Mahato, Sudipta, et al. Generation and Validation of a Leber Congenital Amaurosis, Type 12 Patient-specific IPSC Line (LVPEIi006-B) with a Splice-site Mutation in RD3 and an Isogenic Mutation-corrected IPSC Line (LVPEIi006-B-1). Elsevier.