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. - Guguin J; Besson A; Atmane SN; Yazidi CE; Hadadeh O; Broucqsault N; Magdinier F; Delous M (Stem cell research, 2026)