- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource, 1 online resource.
- Language
-
Englisch
- Bibliographic citation
-
SOAT1 missense variant in two cats with sebaceous gland dysplasia ; volume:298 ; number:4 ; day:15 ; month:4 ; year:2023 ; pages:837-843 ; date:7.2023
Molecular genetics and genomics ; 298, Heft 4 (15.4.2023), 837-843, 7.2023
- Creator
-
Kiener, Sarah
McMahill, Barbara G.
Affolter, Verena K.
Welle, Monika
Yager, Julie A.
Jagannathan, Vidhya
Leeb, Tosso
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1007/s00438-023-02020-6
- URN
-
urn:nbn:de:101:1-2023091208061578487461
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:01 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
- Kiener, Sarah
- McMahill, Barbara G.
- Affolter, Verena K.
- Welle, Monika
- Yager, Julie A.
- Jagannathan, Vidhya
- Leeb, Tosso
- SpringerLink (Online service)
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Missense variant in LOXHD1 is associated with canine nonsyndromic hearing loss
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Heterozygous missense variant in GLI2 impairs human endocrine pancreas development
A dominant missense variant within LMBR1 related to equine polydactyly
The schizophrenia-associated missense variant rs13107325 regulates dendritic spine density
A structural UGDH variant associated with standard Munchkin cats
A rare missense variant in NR1H4 associates with lower cholesterol levels
A missense variant in SLC39A8 is associated with severe idiopathic scoliosis
Autosomal dominant stromal corneal dystrophy associated with a SPARCL1 missense variant
ELN missense variant in patient with mid-aortic syndrome case report
Missense variant in LOXHD1 is associated with canine nonsyndromic hearing loss
Chemoproteogenomic stratification of the missense variant cysteinome
Missense variant contribution to USP9X-female syndrome
Episodic Vestibulocerebellar Ataxia Associated with a CACNA1G Missense Variant
Heterozygous missense variant in GLI2 impairs human endocrine pancreas development
A dominant missense variant within LMBR1 related to equine polydactyly
The schizophrenia-associated missense variant rs13107325 regulates dendritic spine density
A structural UGDH variant associated with standard Munchkin cats
A rare missense variant in NR1H4 associates with lower cholesterol levels
A missense variant in SLC39A8 is associated with severe idiopathic scoliosis
Autosomal dominant stromal corneal dystrophy associated with a SPARCL1 missense variant
ELN missense variant in patient with mid-aortic syndrome case report