Generation of two induced pluripotent stem cell lines from peripheral blood mononuclear cells of a patient with Wilson’s disease

Wilson’s disease is an inherited disorder associated with copper accumulation in the liver, brain and other vital organs. Wilson’s disease is caused by mutations in the ATP7B gene. Over 300 mutations of ATP7B have been described. Despite the disease is autosomal recessive, the patient whose PBMCs we...

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Bibliographic Details
Main Authors: A.A. Malakhova, E.V. Grigor'eva, O.Yu. Vasilyeva, D.I. Zhigalina, N.A. Skryabin, A.A. Sivtcev, N.A. Kolesnikov, A.O. Bueverov, I.N. Lebedev, P.O. Bogomolov, S.M. Zakian
Format: Article
Language:English
Published: Elsevier 2020-08-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506120302233