A synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a cryptic splice event in a Rett syndrome patient
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- 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 synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a cryptic splice event in a Rett syndrome patient ; volume:8 ; number:1 ; day:19 ; month:7 ; year:2013 ; pages:1-7 ; date:12.2013
Orphanet journal of rare diseases ; 8, Heft 1 (19.7.2013), 1-7, 12.2013
- Urheber
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Sheikh, Taimoor I.
- Beteiligte Personen und Organisationen
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Mittal, Kirti
Willis, Mary J.
Vincent, John B.
SpringerLink (Online service)
- DOI
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10.1186/1750-1172-8-108
- URN
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urn:nbn:de:1111-2016050123595
- Rechteinformation
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:53 MESZ
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Beteiligte
- Sheikh, Taimoor I.
- Mittal, Kirti
- Willis, Mary J.
- Vincent, John B.
- SpringerLink (Online service)
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