Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
In: American Journal of Medical Genetics Part A, 170, 6, S. 1502-1509
- Event
-
Veröffentlichung
- (where)
-
Augsburg
- (who)
-
Universität Augsburg
- (when)
-
2016
- Event
-
Veröffentlichung
- (who)
-
Wiley
- (when)
-
2016
- Creator
- DOI
-
10.1002/ajmg.a.37632
- URN
-
urn:nbn:de:bvb:384-opus4-792742
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:27 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
- Evers, Christina
- Kaufmann, Lilian Tamara
- Seitz, Angelika
- Paramasivam, Nagarajan
- Granzow, Martin
- Karch, Stephanie
- Fischer, Christine
- Hinderhofer, Katrin
- Gdynia, Georg
- Elsässer, Michael
- Pinkert, Stefan
- Schlesner, Matthias
- Bartram, Claus R.
- Moog, Ute
- Universität Augsburg
- Wiley
Time of origin
- 2016
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