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Generation of an iPSC line (UMGWi001-B) from a patient with Floating-Harbor Syndrome (FLHS) carrying a heterozygous SRCAP mutation (p.Arg2444).
Franz, M; Hagenau, L; Koch, R; Neubauer, S; Nowack, B; Tzvetkova, A; Jensen, L R; Kuss, A W.
Afiliação
  • Franz M; Human Molecular Genetics Group, Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.
  • Hagenau L; Human Molecular Genetics Group, Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.
  • Koch R; Human Molecular Genetics Group, Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.
  • Neubauer S; SensID GmbH, Rostock, Germany.
  • Nowack B; SensID GmbH, Rostock, Germany.
  • Tzvetkova A; Human Molecular Genetics Group, Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany; Institute of Bioinformatics, University Medicine Greifswald, Greifswald, Germany.
  • Jensen LR; Human Molecular Genetics Group, Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.
  • Kuss AW; Human Molecular Genetics Group, Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany. Electronic address: kussa@uni-greifswald.de.
Stem Cell Res ; 49: 102028, 2020 12.
Article em En | MEDLINE | ID: mdl-33099107
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Anormalidades Craniofaciais / Células-Tronco Pluripotentes Induzidas Limite: Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Anormalidades Craniofaciais / Células-Tronco Pluripotentes Induzidas Limite: Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article