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Induced Pluripotent Stem Cells Derived from a CLN5 Patient Manifest Phenotypic Characteristics of Neuronal Ceroid Lipofuscinoses

Neuronal ceroid lipofuscinoses (NCLs) are autosomal recessive progressive encephalopathies caused by mutations in at least 14 different genes. Despite extensive studies performed in different NCL animal models, the molecular mechanisms underlying neurodegeneration in NCLs remain poorly understood. T...

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Bibliografische gegevens
Gepubliceerd in:Int J Mol Sci
Hoofdauteurs: Uusi-Rauva, Kristiina, Blom, Tea, von Schantz-Fant, Carina, Blom, Tomas, Jalanko, Anu, Kyttälä, Aija
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: MDPI 2017
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5454868/
https://ncbi.nlm.nih.gov/pubmed/28468312
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms18050955
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