Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin C-Reference-Cited by-同舟云学术

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Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin C

Published:2024-04 Issue: Volume:76 Page:103320
ISSN:1873-5061
Container-title:Stem Cell Research
language:en
Short-container-title:Stem Cell Research

Author:

Daya N.M.,Döring K.,Zhuge H.,Volke L.,Stab V.,Dietz J.,Athamneh M.,Roos A.,Zaehres H.,Güttsches A.K.,Mavrommatis L.,Vorgerd M.

Funder

Deutsche Forschungsgemeinschaft

Ruhr-Universität Bochum

Publisher

Elsevier BV

Reference8 articles.

1. Generation of a human iPSC line (HIMRi001-A) from a patient with filaminopathy;Daya;Stem Cell Res.,2023

2. Erythroid differentiation of human induced pluripotent stem cells is independent of donor cell type of origin;Dorn;Haematologica,2015

3. FLNC-associated myofibrillar myopathy: new clinical, functional, and proteomic data;Kley;Neurol. Genet.,2021

4. Clinical and pathological characterization of FLNC-related myofibrillar myopathy caused by founder variant c.8129G>A in Hong Kong Chinese;Lee;Clin. Genet.,2020

5. Myofibrillar myopathies;Selcen;Handb. Clin. Neurol.,2011

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1. In vitro spatiotemporal reconstruction of human skeletal muscle organogenesis;2024-05-12

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