Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease (Englisch)
- Neue Suche nach: Hocking, Lynne J.
- Neue Suche nach: Lucas, Gavin J.A.
- Neue Suche nach: Daroszewska, Anna
- Neue Suche nach: Mangion, Jon
- Neue Suche nach: Olavesen, Mark
- Neue Suche nach: Cundy, Tim
- Neue Suche nach: Nicholson, Geoff C.
- Neue Suche nach: Ward, Lynley
- Neue Suche nach: Bennett, Simon T.
- Neue Suche nach: Wuyts, Wim
- Neue Suche nach: Van Hul, Wim
- Neue Suche nach: Ralston, Stuart H.
- Neue Suche nach: Hocking, Lynne J.
- Neue Suche nach: Lucas, Gavin J.A.
- Neue Suche nach: Daroszewska, Anna
- Neue Suche nach: Mangion, Jon
- Neue Suche nach: Olavesen, Mark
- Neue Suche nach: Cundy, Tim
- Neue Suche nach: Nicholson, Geoff C.
- Neue Suche nach: Ward, Lynley
- Neue Suche nach: Bennett, Simon T.
- Neue Suche nach: Wuyts, Wim
- Neue Suche nach: Van Hul, Wim
- Neue Suche nach: Ralston, Stuart H.
In:
Human molecular genetics
;
11
, 22
;
2735-
;
2002
- Aufsatz (Zeitschrift) / Elektronische Ressource
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Titel:Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease
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Beteiligte:Hocking, Lynne J. ( Autor:in ) / Lucas, Gavin J.A. ( Autor:in ) / Daroszewska, Anna ( Autor:in ) / Mangion, Jon ( Autor:in ) / Olavesen, Mark ( Autor:in ) / Cundy, Tim ( Autor:in ) / Nicholson, Geoff C. ( Autor:in ) / Ward, Lynley ( Autor:in ) / Bennett, Simon T. ( Autor:in ) / Wuyts, Wim ( Autor:in )
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Erschienen in:Human molecular genetics ; 11, 22 ; 2735-
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Verlag:
- Neue Suche nach: Oxford University Press
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Erscheinungsdatum:15.10.2002
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ISSN:
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DOI:
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Medientyp:Aufsatz (Zeitschrift)
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Format:Elektronische Ressource
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Sprache:Englisch
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Datenquelle:
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