Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1432-1203
- 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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Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency ; volume:126 ; number:3 ; day:23 ; month:5 ; year:2009 ; pages:449-456 ; date:9.2009
Human genetics; 126, Heft 3 (23.5.2009), 449-456, 9.2009
- Urheber
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Pintao, Maria C.
Garcia, A. A.
Borgel, D.
Alhenc-Gelas, M.
Spek, C. A.
Visser, M. C. H. de
Gandrille, S.
Reitsma, Pieter H.
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1007/s00439-009-0687-9
- URN
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urn:nbn:de:101:1-2019050516324879999368
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:48 MESZ
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Beteiligte
- Pintao, Maria C.
- Garcia, A. A.
- Borgel, D.
- Alhenc-Gelas, M.
- Spek, C. A.
- Visser, M. C. H. de
- Gandrille, S.
- Reitsma, Pieter H.
- SpringerLink (Online service)
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