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An induced pluripotent stem cell line (TRNDi001-D) from a Niemann-Pick disease type C1 (NPC1) patient carrying a homozygous p. I1061T (c. 3182T>C) mutation in the NPC1 gene

Niemann-Pick disease, type C (NPC) is a rare autosomal recessive genetic disease caused by mutations in either NPC1 or NPC2, which encodes an intracellular cholesterol-binding protein in lysosome. Deficiency of either NPC1 or NPC2 protein results in malfunction of intracellular cholesterol trafficki...

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Detalhes bibliográficos
Publicado no:Stem Cell Res
Main Authors: Li, Rong, Pradhan, Manisha, Xu, Miao, Roeder, Amanda, Beers, Jeanette, Zou, Jizhong, Liu, Chengyu, Porter, Forbes D., Zheng, Wei
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7218921/
https://ncbi.nlm.nih.gov/pubmed/32114296
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.scr.2020.101737
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