Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2431
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report ; volume:20 ; number:1 ; day:3 ; month:9 ; year:2020 ; pages:1-5 ; date:12.2020
BMC pediatrics ; 20, Heft 1 (3.9.2020), 1-5, 12.2020
- Urheber
-
Zeng, Ting
Liao, Linyan
Guo, Yi
Liu, Xuxu
Xiong, Xiaobo
Zhang, Yu
Cen, Shi
Li, Honghui
Wei, Shuzhang
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s12887-020-02309-0
- URN
-
urn:nbn:de:101:1-2020102419365452683393
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:38 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
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Beteiligte
- Zeng, Ting
- Liao, Linyan
- Guo, Yi
- Liu, Xuxu
- Xiong, Xiaobo
- Zhang, Yu
- Cen, Shi
- Li, Honghui
- Wei, Shuzhang
- SpringerLink (Online service)
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