A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1617-4623
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle ; volume:296 ; number:6 ; day:2 ; month:10 ; year:2021 ; pages:1313-1322 ; date:11.2021
Molecular genetics and genomics ; 296, Heft 6 (2.10.2021), 1313-1322, 11.2021
- Creator
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Jacinto, Joana G. P.
Häfliger, Irene M.
Veiga, Inês M. B.
Letko, Anna
Gentile, Arcangelo
Drögemüller, Cord
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s00438-021-01824-8
- URN
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urn:nbn:de:101:1-2022011519201653011519
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:39 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
- Jacinto, Joana G. P.
- Häfliger, Irene M.
- Veiga, Inês M. B.
- Letko, Anna
- Gentile, Arcangelo
- Drögemüller, Cord
- SpringerLink (Online service)
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The use of molecular genetics in eliminating of inherited anomalies in cattle
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A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle
De Hepatomphalocele Congenita
De syphilitide congenita
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Paramyotonia congenita (Eulenburg)
Ueber Phimosis congenita
A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle
A frameshift mutation in GON4L is associated with proportionate dwarfism in Fleckvieh cattle
Carriers of a novel frame-shift insertion in WNT16a possess elevatedpancreatic expression of TCF7L2
Insertion/deletion-activated frame-shift fluorescence protein is a sensitive reporter for genomic DNA editing
The use of molecular genetics in eliminating of inherited anomalies in cattle
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