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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.

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Bibliographic Details
Title:	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.
Authors:	Guguin J; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon, CRNL U1028 UMR5292, GENDEV, Bron, France., Besson A; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon, CRNL U1028 UMR5292, GENDEV, Bron, France., Atmane SN; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France., Yazidi CE; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France., Hadadeh O; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France., Broucqsault N; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France., Magdinier F; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France., Delous M; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon, CRNL U1028 UMR5292, GENDEV, Bron, France. Electronic address: marion.delous@inserm.fr.
Source:	Stem cell research [Stem Cell Res] 2026 Apr; Vol. 92, pp. 103940. Date of Electronic Publication: 2026 Feb 16.
Publication Type:	Journal Article; Case Reports
Journal Info:	Publisher: Elsevier Country of Publication: England NLM ID: 101316957 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1876-7753 (Electronic) Linking ISSN: 18735061 NLM ISO Abbreviation: Stem Cell Res Subsets: MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	1876-7753
DOI:	10.1016/j.scr.2026.103940