Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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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
- Creator
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Ling, Chao
Sui, Ruifang
Yao, Fengxia
Wu, Zhihong
Zhang, Xue
Zhang, Shuyang
- Contributor
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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
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:56 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Ling, Chao
- Sui, Ruifang
- Yao, Fengxia
- Wu, Zhihong
- Zhang, Xue
- Zhang, Shuyang
- SpringerLink (Online service)
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