Generation of the human induced pluripotent stem cell line (UKWNLi001-A) from skin fibroblasts of a woman with Fabry disease carrying the X-chromosomal heterozygous c.708 G > C (W236C) missense mutation in exon 5 of the alpha-galactosidase–A gene

Similar Items

• Generation of the human induced pluripotent stem cell line UKWNLi002-A from dermal fibroblasts of a woman with a heterozygous c.608 C>T (p.Thr203Met) mutation in exon 3 of the nerve growth factor gene potentially associated with hereditary sensory and autonomic neuropathy type 5
  by: Thomas Klein, et al.
  Published: (2018-12-01)
• Affective and cognitive behavior in the alpha-galactosidase A deficient mouse model of Fabry disease.
  by: Lukas Hofmann, et al.
  Published: (2017-01-01)
• A Missense Mutation of the α-Galactosidase A Gene in a Chinese Family of Fabry Disease with Renal Failure
  by: Chunli Wang, et al.
  Published: (2013-06-01)
• Generation of two induced pluripotent stem cell lines from skin fibroblasts of sisters carrying a c.1094C>A variation in the SCN10A gene potentially associated with small fiber neuropathy
  by: Thomas Klein, et al.
  Published: (2019-03-01)
• Generation of pulmonary arterial hypertension patient-specific induced pluripotent stem cell lines from three unrelated patients with a heterozygous missense mutation in exon 12, a heterozygous in-frame deletion in exon 3 and a missense mutation in exon 11 of the BMPR2 gene
  by: Abdulai Usman, et al.
  Published: (2021-08-01)