Production of an induced pluripotent stem cell line CSSi018-A (14192) from a patient with hypomyelinating leukodystrophy 7 (HLD7) carrying biallelic variants of POLR3A (c.1802 T > A; c.4072G > A)

Hypomyelinating leukodystrophies (HLD) are a group of heterogeneous genetic disorders characterized by a deficit in myelin deposition during brain development. Specifically, 4H-Leukodystrophy is a recessive disease due to biallelic mutations in the POLR3A gene, which encodes one of the subunits form...

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Veröffentlicht in:Stem cell research 2024-08, Vol.78, p.103468, Article 103468
Hauptverfasser: Casamassa, Alessia, Rotundo, Giovannina, Ceresoni, Chiara, Turco, Elisa Maria, Torrente, Isabella, Candido, Ornella, Nicita, Francesco, Tonduti, Davide, Bertini, Enrico, Marano, Massimo, Ferrari, Daniela, Cereda, Cristina, Pennuto, Maria, Vescovi, Angelo Luigi, Carelli, Stephana, Rosati, Jessica
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Sprache:eng
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Zusammenfassung:Hypomyelinating leukodystrophies (HLD) are a group of heterogeneous genetic disorders characterized by a deficit in myelin deposition during brain development. Specifically, 4H-Leukodystrophy is a recessive disease due to biallelic mutations in the POLR3A gene, which encodes one of the subunits forming the catalytic core of RNA polymerase III (PolIII). The disease also presents non-neurological signs such as hypodontia and hypogonadotropic hypogonadism. Here, we report the generation of a human induced pluripotent stem cell (hiPSC) line from fibroblasts of the first identified carrier of the biallelic POLR3A variants c.1802 T > A and c.4072G > A.
ISSN:1873-5061
1876-7753
1876-7753
DOI:10.1016/j.scr.2024.103468