Generation of two induced pluripotent stem cell lines (HIMRi006-A and HIMRi007-A) from Pompe patients with infantile and late disease onset

Author:

Volke L.,Daya N.M.,Döring K.,Rohm M.,Athamneh M.,Zaehres H.,Roos A.,Güttsches A.K.,Mavrommatis L.,Vorgerd M.

Funder

Deutsche Forschungsgemeinschaft

Ruhr-Universität Bochum

Publisher

Elsevier BV

Reference6 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. Carrier frequency and predicted genetic prevalence of Pompe disease based on a general population database;Park;Mol. Genet. Metab. Rep.,2021

4. null On Behalf Of The Pompe Registry Sites, GAA variants and phenotypes among 1,079 patients with Pompe disease: Data from the Pompe Registry;Reuser;Hum. Mutat.,2019

5. Genetic basis of hypertrophic cardiomyopathy in children;Rupp;Clin. Res. Cardiol.,2019

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