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Generation of an iPSC line from a patient with tyrosine hydroxylase (TH) deficiency: TH-1 iPSC.
Jung-Klawitter, Sabine; Blau, Nenad; Sebe, Attila; Ebersold, Juliane; Göhring, Gudrun; Opladen, Thomas.
Affiliation
  • Jung-Klawitter S; Department of General Pediatrics, Division of Neuropediatrics and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany. Electronic address: sabine.jung-klawitter@med.uni-heidelberg.de.
  • Blau N; Department of General Pediatrics, Division of Neuropediatrics and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Sebe A; Paul-Ehrlich Institute, Langen, Germany.
  • Ebersold J; Department of Human Genetics, Hannover Medical School (MHH), Hannover, Germany.
  • Göhring G; Department of Human Genetics, Hannover Medical School (MHH), Hannover, Germany.
  • Opladen T; Department of General Pediatrics, Division of Neuropediatrics and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany.
Stem Cell Res ; 17(3): 580-583, 2016 11.
Article in En | MEDLINE | ID: mdl-27934587
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tyrosine 3-Monooxygenase / Dystonic Disorders / Induced Pluripotent Stem Cells Type of study: Prognostic_studies Limits: Humans / Male Language: En Journal: Stem Cell Res Year: 2016 Document type: Article Country of publication: United kingdom
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tyrosine 3-Monooxygenase / Dystonic Disorders / Induced Pluripotent Stem Cells Type of study: Prognostic_studies Limits: Humans / Male Language: En Journal: Stem Cell Res Year: 2016 Document type: Article Country of publication: United kingdom