Production and characterization of human induced pluripotent stem cells (iPSC) CSSi007-A (4383) from Joubert Syndrome

Joubert syndrome (JS) is an autosomal recessive neurodevelopmental disorder, characterized by congenital cerebellar and brainstem defects, belonging to the group of disorders known as ciliopathies, which are caused by mutations in genes encoding proteins of the primary cilium and basal body. Human i...

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Detalhes bibliográficos
Publicado no:Stem Cell Res
Main Authors: Altieri, Filomena, D'Anzi, Angela, Martello, Francesco, Tardivo, Silvia, Spasari, Iolanda, Ferrari, Daniela, Bernardini, Laura, Lamorte, Giuseppe, Mazzoccoli, Gianluigi, Valente, Enza Maria, Vescovi, Angelo Luigi, Rosati, Jessica
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6617992/
https://ncbi.nlm.nih.gov/pubmed/31202121
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.scr.2019.101480
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