APA (7th ed.) Citation

J, G., A, B., SN, A., CE, Y., O, H., N, B., . . . M, D. (2026). Generation of the iPSC line CRNLi001-A from a patient with microcephaly and harbouring the most recurrent RTTN variant, c.2953A>G, at homozygous state. Stem cell research, 92, 103940. https://doi.org/10.1016/j.scr.2026.103940

Chicago Style (17th ed.) Citation

J, Guguin, Besson A, Atmane SN, Yazidi CE, Hadadeh O, Broucqsault N, Magdinier F, and Delous M. "Generation of the IPSC Line CRNLi001-A from a Patient with Microcephaly and Harbouring the Most Recurrent RTTN Variant, C.2953A>G, at Homozygous State." Stem Cell Research 92 (2026): 103940. https://doi.org/10.1016/j.scr.2026.103940.

MLA (9th ed.) Citation

J, Guguin, et al. "Generation of the IPSC Line CRNLi001-A from a Patient with Microcephaly and Harbouring the Most Recurrent RTTN Variant, C.2953A>G, at Homozygous State." Stem Cell Research, vol. 92, 2026, p. 103940, https://doi.org/10.1016/j.scr.2026.103940.