Identification of two novel null variants in CLN8 by targeted next-generation sequencing: first report of a Chinese patient with neuronal ceroid lipofuscinosis due to CLN8 variants
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- 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 two novel null variants in CLN8 by targeted next-generation sequencing: first report of a Chinese patient with neuronal ceroid lipofuscinosis due to CLN8 variants ; volume:19 ; number:1 ; day:8 ; month:2 ; year:2018 ; pages:1-6 ; date:12.2018
BMC medical genetics ; 19, Heft 1 (8.2.2018), 1-6, 12.2018
- Schlagwort
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Erbkrankheit
Erbschaden
- Urheber
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Gao, Zhijie
- Beteiligte Personen und Organisationen
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Xie, Hua
Jiang, Qian
Wu, Nan
Chen, Xiaoli
Chen, Qian
SpringerLink (Online service)
- DOI
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10.1186/s12881-018-0535-7
- URN
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urn:nbn:de:1111-201804157382
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:55 MESZ
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Beteiligte
- Gao, Zhijie
- Xie, Hua
- Jiang, Qian
- Wu, Nan
- Chen, Xiaoli
- Chen, Qian
- SpringerLink (Online service)
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