Article
Human induced pluripotent stem cell line (ONHi001-A) generated from a patient with infantile neuroaxonal dystrophy having PLA2G6 c.517C > T (p.Q173X) and c.1634A > G (p.K545R) compound heterozygous mutations.
Stem cell research - 1 Jun 2023
Fukusumi Hayato, Togo Kazuyuki, Beck Goichi, Shofuda Tomoko, Kanematsu Daisuke, Yamamoto Atsuyo, Sumida Miho, Baba Kousuke, Mochizuki Hideki, Kanemura Yonehiro
Abstract excerpt
Infantile neuroaxonal dystrophy (INAD) is a rare neurodegenerative disease caused mainly by homozygous or compound heterozygous mutations in the PLA2G6 gene. We generated a human induced pluripotent stem cell (hiPSC) line (ONHi001-A) using fibroblasts derived from a patient with INAD. The patient exhibited c.517C > T (p.Q173X) and c.1634A > G (p.K545R) compound heterozygous mutations in the PLA2G6 gene. This...
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