SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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In: European Journal of Human Genetics, 23, 12, S. 1627-1633
- Ereignis
-
Veröffentlichung
- (wo)
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Augsburg
- (wer)
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Universität Augsburg
- (wann)
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2015
- Ereignis
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Veröffentlichung
- (wer)
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Springer Science and Business Media LLC
- (wann)
-
2015
- Urheber
- DOI
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10.1038/ejhg.2015.46
- URN
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urn:nbn:de:bvb:384-opus4-792823
- Rechteinformation
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:24 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
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Beteiligte
- 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
Entstanden
- 2015
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