SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
In: European Journal of Human Genetics, 23, 12, S. 1627-1633
- Event
-
Veröffentlichung
- (where)
-
Augsburg
- (who)
-
Universität Augsburg
- (when)
-
2015
- Event
-
Veröffentlichung
- (who)
-
Springer Science and Business Media LLC
- (when)
-
2015
- Creator
- DOI
-
10.1038/ejhg.2015.46
- URN
-
urn:nbn:de:bvb:384-opus4-792823
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:24 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
- Paramasivam, Nagarajan
- Hinderhofer, Katrin
- Fischer, Christine
- Granzow, Martin
- Schmidt-Bacher, Annette
- Eils, Roland
- Steinbeisser, Herbert
- Schlesner, Matthias
- Moog, Ute
- Universität Augsburg
- Springer Science and Business Media LLC
Time of origin
- 2015
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