Establishment of an induced pluripotent stem cell (iPSC) line SDQLCHi045-A from peripheral blood mononuclear cells of a patient with Coffin-Siris syndrome 1 carrying a mutation in ARID1B gene

Coffin-Siris syndrome 1 (CSS1) is a multiple malformation syndrome characterized by mental retardation associated with coarse facial features, hypertrichosis, sparse scalp hair, and hypoplastic or absent fifth fingernails or toenails. Mutations in the ARID1B gene are the most common cause of CSS1. H...

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Bibliographic Details
Main Authors: Xiaomeng Yang, Chen Liu, Haiyan Zhang, Yuqiang Lv, Yue Li, Zilong Li, Yi Liu, Zhongtao Gai
Format: Article
Language:English
Published: Elsevier 2023-02-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506122003312