Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1756-994X
- 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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Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders ; volume:11 ; number:1 ; day:25 ; month:10 ; year:2019 ; pages:1-14 ; date:12.2019
Genome medicine ; 11, Heft 1 (25.10.2019), 1-14, 12.2019
- Urheber
-
Chow, Julie
Jensen, Matthew
Amini, Hajar
Hormozdiari, Farhad
Penn, Osnat
Shifman, Sagiv
Girirajan, Santhosh
Hormozdiari, Fereydoun
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1186/s13073-019-0678-y
- URN
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urn:nbn:de:101:1-2020021722075194908285
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:47 MESZ
Datenpartner
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Beteiligte
- Chow, Julie
- Jensen, Matthew
- Amini, Hajar
- Hormozdiari, Farhad
- Penn, Osnat
- Shifman, Sagiv
- Girirajan, Santhosh
- Hormozdiari, Fereydoun
- SpringerLink (Online service)
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