A novel TPM2 gene splice-site mutation causes severe congenital myopathy with arthrogryposis and dysmorphic features
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2190-3883
- 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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A novel TPM2 gene splice-site mutation causes severe congenital myopathy with arthrogryposis and dysmorphic features ; volume:58 ; number:2 ; day:10 ; month:10 ; year:2016 ; pages:199-203 ; date:5.2017
Journal of applied genetics ; 58, Heft 2 (10.10.2016), 199-203, 5.2017
- Schlagwort
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Erbkrankheit
Erbschaden
- Urheber
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Mroczek, Magdalena
- Beteiligte Personen und Organisationen
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Kabzińska, Dagmara
Chrzanowska, Krystyna H.
Pronicki, Maciej
Kochański, Andrzej
SpringerLink (Online service)
- DOI
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10.1007/s13353-016-0368-z
- URN
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urn:nbn:de:1111-2017043001
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:36 MESZ
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Beteiligte
- Mroczek, Magdalena
- Kabzińska, Dagmara
- Chrzanowska, Krystyna H.
- Pronicki, Maciej
- Kochański, Andrzej
- SpringerLink (Online service)
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