Identification of a familial cleidocranial dysplasia with a novel RUNX2 mutation and establishment of patient-derived induced pluripotent stem cells
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1618-1255
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Identification of a familial cleidocranial dysplasia with a novel RUNX2 mutation and establishment of patient-derived induced pluripotent stem cells ; day:15 ; month:11 ; year:2021 ; pages:1-8
Odontology ; (15.11.2021), 1-8
- Urheber
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Hamada, Atsuko
Mukasa, Hanae
Taguchi, Yuki
Akagi, Eri
Obayashi, Fumitaka
Yamasaki, Sachiko
Kanda, Taku
Koizumi, Koichi
Toratani, Shigeaki
Okamoto, Tetsuji
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1007/s10266-021-00674-5
- URN
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urn:nbn:de:101:1-2022012522153665581240
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:40 MESZ
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Beteiligte
- Hamada, Atsuko
- Mukasa, Hanae
- Taguchi, Yuki
- Akagi, Eri
- Obayashi, Fumitaka
- Yamasaki, Sachiko
- Kanda, Taku
- Koizumi, Koichi
- Toratani, Shigeaki
- Okamoto, Tetsuji
- SpringerLink (Online service)
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Modelling neurological diseases using patientderived induced pluripotent stem cells
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