Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2474
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study ; volume:17 ; number:1 ; day:9 ; month:11 ; year:2016 ; pages:1-6 ; date:12.2016
BMC musculoskeletal disorders ; 17, Heft 1 (9.11.2016), 1-6, 12.2016
- Creator
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Cardinale, Christopher J.
- Contributor
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Li, Dong
Tian, Lifeng
Connolly, John J.
March, Michael E.
Hou, Cuiping
Wang, Fengxiang
Snyder, James
Kim, Cecilia E.
Chiavacci, Rosetta M.
Sleiman, Patrick M.
Burnham, Jon M.
Hákon Hákonarson
SpringerLink (Online service)
- DOI
-
10.1186/s12891-016-1320-4
- URN
-
urn:nbn:de:1111-2016120216210
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:45 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
- Cardinale, Christopher J.
- Li, Dong
- Tian, Lifeng
- Connolly, John J.
- March, Michael E.
- Hou, Cuiping
- Wang, Fengxiang
- Snyder, James
- Kim, Cecilia E.
- Chiavacci, Rosetta M.
- Sleiman, Patrick M.
- Burnham, Jon M.
- Hákon Hákonarson
- SpringerLink (Online service)
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