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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617992/
https://www.ncbi.nlm.nih.gov/pubmed/31202121
http://dx.doi.org/10.1016/j.scr.2019.101480

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