Title |
SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract / Christina Evers, Nagarajan Paramasivam, Katrin Hinderhofer, Christine Fischer, Martin Granzow, Annette Schmidt-Bacher, Roland Eils, Herbert Steinbeisser, Matthias Schlesner, Ute Moog |
|---|---|
Involved |
Christina Evers (Verfasser)
Nagarajan Paramasivam (Verfasser) Katrin Hinderhofer (Verfasser) Christine Fischer (Verfasser)
Martin Granzow (Verfasser)
Annette Schmidt-Bacher (Verfasser) Roland Eils (Verfasser) Herbert Steinbeisser (Verfasser) Matthias Schlesner (Verfasser) Ute Moog (Verfasser) |
Published |
Augsburg: Universität Augsburg |
Extent |
Online-Ressource |
Language |
|
Country |
|
Topic |
|
DDC notation |
|
Persistent identifier |
urn:nbn:de:bvb:384-opus4-792823 (URN) |
Further information |
In: European Journal of Human Genetics, 23, 12, S. 1627-1633 |
Record ID |
1252246781 |
Please note
The beta version does not yet contain all functions and information of the DNB portal catalogue. If you are missing information or want to order a medium, please visit the page in the DNB portal catalogue via the following link: