Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome
- 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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Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome ; volume:20 ; number:1 ; day:14 ; month:1 ; year:2019 ; pages:1-7 ; date:12.2019
BMC medical genetics ; 20, Heft 1 (14.1.2019), 1-7, 12.2019
- Urheber
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Ling, Chao
Sui, Ruifang
Yao, Fengxia
Wu, Zhihong
Zhang, Xue
Zhang, Shuyang
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s12881-018-0725-3
- URN
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urn:nbn:de:101:1-2019021922151378199545
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:56 MESZ
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Beteiligte
- Ling, Chao
- Sui, Ruifang
- Yao, Fengxia
- Wu, Zhihong
- Zhang, Xue
- Zhang, Shuyang
- SpringerLink (Online service)
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