Generation of a human induced pluripotent stem cell (iPSC) line (JUCTCi019-A) from a patient with Charcot-Marie-Tooth disease type 2A2 (CMT2A2) due to a heterozygous missense substitution c.2119C > T (p.Arg707Trp) in MFN2 gene

Charcot-Marie-Tooth disease (CMT) is an inherited neurological disorder characterized by the progressive damage of the peripheral nerves. We generated a human induced pluripotent stem cell (iPSC) line JUCTCi019-A using dermal fibroblasts-derived from a 50-year-old CMT2A2 patient carrying a heterozyg...

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Bibliographic Details
Main Authors:	A. Ismail, M. (Author), Ababneh, N.A (Author), Abdulelah, A.A (Author), Ali, D. (Author), Al-Kurdi, B. (Author), Awidi, A. (Author), Barham, R. (Author), Hadidi, S.A (Author), Hassona, Y. (Author), Madadha, A. (Author), Masri, A. (Author), Muamar, A.S.H (Author), Sallam, M. (Author)
Format:	Article
Language:	English
Published:	Elsevier B.V. 2022
Online Access:	View Fulltext in Publisher

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Generation of a human induced pluripotent stem cell (iPSC) line (JUCTCi019-A) from a patient with Charcot-Marie-Tooth disease type 2A2 (CMT2A2) due to a heterozygous missense substitution c.2119C > T (p.Arg707Trp) in MFN2 gene

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