Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1756-994X
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
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
- Creator
-
Chow, Julie
Jensen, Matthew
Amini, Hajar
Hormozdiari, Farhad
Penn, Osnat
Shifman, Sagiv
Girirajan, Santhosh
Hormozdiari, Fereydoun
- Contributor
-
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
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:47 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Chow, Julie
- Jensen, Matthew
- Amini, Hajar
- Hormozdiari, Farhad
- Penn, Osnat
- Shifman, Sagiv
- Girirajan, Santhosh
- Hormozdiari, Fereydoun
- SpringerLink (Online service)
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