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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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
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  Data: 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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  Data: <searchLink fieldCode="AU" term="%22Guguin+J%22">Guguin J</searchLink>; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon, CRNL U1028 UMR5292, GENDEV, Bron, France.<br /><searchLink fieldCode="AU" term="%22Besson+A%22">Besson A</searchLink>; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon, CRNL U1028 UMR5292, GENDEV, Bron, France.<br /><searchLink fieldCode="AU" term="%22Atmane+SN%22">Atmane SN</searchLink>; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Yazidi+CE%22">Yazidi CE</searchLink>; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Hadadeh+O%22">Hadadeh O</searchLink>; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Broucqsault+N%22">Broucqsault N</searchLink>; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Magdinier+F%22">Magdinier F</searchLink>; Aix Marseille Univ, INSERM, MMG, U1251, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Delous+M%22">Delous M</searchLink>; 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.
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      – TitleFull: 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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