Generation of an iPSC line (SMCPGi001-A) from a patient with Bain type X-linked mental retardation syndrome carrying HNRNPH2 gene mutation

Summary

Bain type X-linked mental retardation syndrome is an X-linked dominant neurodevelopmental disorder characterized by psychomotor developmental delay and intellectual disability. The rare syndrome is caused by HNRNPH2 gene mutation. In this study, the iPSC cell line (SMCPGi001-A) was acquired by Sendai virus-mediated iPSC reprogramming from the peripheral blood mononuclear cells (PBMCs) obtained from a 1-year-old girl with de novo p.R206W mutation in the HNRNPH2 gene. The identification experiments of stemness and differentiation potential of three germ layers showed that the cell line had pluripotent stem cell characteristics and the potential of tridermal differentiation. Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.

Authors Ma X, Zhu L, Chen W, Sheng M, Peng F, Liang M, Zhao Y, Wang Y, Feng Z
Journal Stem cell research
Publication Date 2021 Oct 23;57:102571
PubMed 34763229
DOI 10.1016/j.scr.2021.102571

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