Zeitschriftenaufsatz
|
2011
An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle.
Autor:in
Drögemüller, Cord; Reichart, Ursula; Seuberlich, Torsten; Oevermann, Anna; Baumgartner, Martin; Kühni Boghenbor, Kathrin; Stoffel, Michael H; Syring, Claudia; Meylan, Mireille; Müller, Simone; Müller, Mathias; Gredler, Birgit; Sölkner, Johann; Leeb, Tosso;
Publikationen als Autor:in / Herausgeber:in der Vetmeduni
Journal
Schlagwörter
Animals; Axons/metabolism; Axons/pathology*; Cattle; Cattle Diseases/genetics*; Cattle Diseases/pathology; Chromosome Mapping; DNA Mutational Analysis; Gene Expression Regulation; Genetic Predisposition to Disease*; Genome-Wide Association Study; Homozygote; Humans; Inheritance Patterns/genetics; Mitochondria/metabolism; Mitochondria/ultrastructure; Mitochondrial Proteins/genetics*; Mitochondrial Proteins/metabolism; Molecular Sequence Data; Muscle Fibers, Skeletal/pathology; Muscle Fibers, Skeletal/ultrastructure; Mutation/genetics*; Nerve Degeneration/genetics*; Nerve Degeneration/pathology; Phenotype; RNA Splice Sites/genetics*; RNA, Messenger/genetics; RNA, Messenger/metabolism;
Dokumententyp
Originalarbeit
ISSN/eISSN
1932-6203 -
10.1371/journal.pone.0018931
WoS ID
PubMed ID
Titel des Sammelwerks
PLOS ONE;