iPSC reprogramming of fibroblasts from a patient with a Rothmund-Thomson syndrome RTS

iPSC reprogramming of fibroblasts from a patient with a Rothmund-Thomson syndrome RTS

Rothmund-Thomson Syndrome (RTS) is a rare autosomal recessive disease that manifests several clinical features of accelerated aging. These findings include atrophic skin and pigment changes, alopecia, osteopenia, cataracts, and an increased incidence of cancer for patients. Mutations in RECQL4 gene...

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Bibliographic Details
Main Authors: Vincent Gatinois, Romain Desprat, Lydiane Pichard, Fabienne Becker, Alice Goldenberg, Xavier Balguerie, Franck Pellestor, Jean-Marc Lemaitre
Format: Article
Language:English
Published: Elsevier 2020-05-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506120301094

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http://www.sciencedirect.com/science/article/pii/S1873506120301094

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