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A Missense Variant in ALDH5A1 Associated with Canine Succin..:
Vernau, Karen M
;
Struys, Eduard
;
Letko, Anna
...
qt0jn6h55t. , 2020
Link:
https://escholarship.org/uc/item/0jn6h55t
RT Journal T1
A Missense Variant in ALDH5A1 Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt0jn6h55t&Exemplar=1&LAN=DE A1 Vernau, Karen M A1 Struys, Eduard A1 Letko, Anna A1 Woolard, Kevin D A1 Aguilar, Miriam A1 Brown, Emily A A1 Cissell, Derek D A1 Dickinson, Peter J A1 Shelton, G Diane A1 Broome, Michael R A1 Gibson, K Michael A1 Pearl, Phillip L A1 König, Florian A1 Van Winkle, Thomas J A1 O'Brien, Dennis A1 Roos, B A1 Matiasek, Kaspar A1 Jagannathan, Vidhya A1 Drögemüller, Cord A1 Mansour, Tamer A A1 Brown, C Titus A1 Bannasch, Danika L PB eScholarship, University of California YR 2020 K1 Brain K1 Cerebrospinal Fluid K1 Animals K1 Dogs K1 Seizures K1 Amino Acid Metabolism K1 Inborn Errors K1 Disease Models K1 Animal K1 gamma-Aminobutyric Acid K1 Developmental Disabilities K1 Amino Acid Sequence K1 Phenotype K1 Mutation K1 Missense K1 Female K1 Male K1 Succinate-Semialdehyde Dehydrogenase K1 Metabolic Networks and Pathways K1 Genome-Wide Association Study K1 Genetic Testing K1 4-hydroxybutyric acid K1 ALDH5A1 K1 GABA K1 GWAS K1 SSADHD K1 encephalopathy K1 inborn error of metabolism K1 inherited K1 precision medicine K1 succinic semialdehyde K1 whole-genome sequencing K1 Orphan Drug K1 Rare Diseases K1 Brain Disorders K1 Genetics K1 Neurosciences K1 Biotechnology K1 Human Genome K1 2.1 Biological and endogenous factors K1 Aetiology K1 Neurological JF qt0jn6h55t LK http://dx.doi.org/https://escholarship.org/uc/item/0jn6h55t DO https://escholarship.org/uc/item/0jn6h55t SF ELIB - SuUB Bremen
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