Generation and genetic repair of two human induced pluripotent stem cell lines from patients with Epidermolysis Bullosa simplex associated with a heterozygous mutation in the translation initiation codon of KLHL24
Author:
Funder
Novo Nordisk Foundation
DEBRA Austria
Publisher
Elsevier BV
Reference6 articles.
1. Lymphoblast-derived hiPS cell lines generated from four individuals of a family of genetically unrelated parents and their female monozygotic twins;Bouma;Stem Cell Res.,2019
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3. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility;Has;Br. J. Dermatol.,2020
4. Development of defective and persistent Sendai virus vector: a unique gene delivery/expression system ideal for cell reprogramming;Nishimura;J. Biol. Chem.,2011
5. Generation and genetic repair of two human induced pluripotent cell lines from patients with Epidermolysis Bullosa simplex and dilated cardiomyopathy associated with a heterozygous mutation in the translation initiation codon of KLHL24;Ramovs;Stem Cell Res.,2021
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