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dc.contributor.editorBannasch, Danika
dc.contributor.editorFriedenberg, Steven
dc.date.accessioned2021-05-01T15:14:40Z
dc.date.available2021-05-01T15:14:40Z
dc.date.issued2021
dc.identifierONIX_20210501_9783036504728_303
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/68557
dc.description.abstractThis book includes a collection of publications describing the molecular etiology of inherited diseases and conditions in companion animals (dogs and cats). In addition to contributing to the health of companion animals, this research also benefits humans that have similar types of diseases.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: generalen_US
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PS Biology, life sciencesen_US
dc.subject.otherCanis familiaris
dc.subject.otherdermatology
dc.subject.otherimmunology
dc.subject.otheranimal model
dc.subject.otherskin
dc.subject.otherTLR7
dc.subject.othertoll-like receptor
dc.subject.othersyndecan binding protein
dc.subject.othersyntenin-1
dc.subject.othersystemic lupus erythematosus
dc.subject.otherSLE
dc.subject.otherCLE
dc.subject.otherwhole-genome sequencing
dc.subject.othercraniomandibular osteopathy
dc.subject.othercalvarial hyperostotic syndrome
dc.subject.otherCaffey disease
dc.subject.otherinfantile cortical hyperostosis
dc.subject.otherrare disease
dc.subject.otherSLC37A2
dc.subject.otherCOL1A1
dc.subject.otherSLC35D1
dc.subject.otherCanis lupus familiaris
dc.subject.otherwhole-genome sequence
dc.subject.othergenodermatosis
dc.subject.otherkeratinocyte
dc.subject.otherSAM syndrome
dc.subject.otherprecision medicine
dc.subject.otherdog
dc.subject.otherdesmosome
dc.subject.otheracantholysis
dc.subject.othercalcium
dc.subject.otherveterinary medicine
dc.subject.otherfeline
dc.subject.otherFelis catus
dc.subject.otherbrain malformation
dc.subject.otherBMP12
dc.subject.otherneurodevelopment
dc.subject.othergenetics
dc.subject.othergenomics
dc.subject.othermendelian traits
dc.subject.othergenome-wide association study
dc.subject.otherwhole genome sequencing
dc.subject.othermitochondrion
dc.subject.otherphosphoenolpyruvate-carboxykinase
dc.subject.otherinborn error of metabolism
dc.subject.otherencephalopathy
dc.subject.otherSSADHD
dc.subject.otherALDH5A1
dc.subject.otherGABA
dc.subject.other4-hydroxybutyric acid
dc.subject.othersuccinic semialdehyde
dc.subject.otherGWAS
dc.subject.otherinherited
dc.subject.otherwhole genome sequence
dc.subject.otherwgs
dc.subject.otherlaminin
dc.subject.otherBardet–Biedl syndrome (BBS)
dc.subject.otherprimary cilia
dc.subject.otherciliopathy
dc.subject.otherBBS8
dc.subject.otherprogressive retinal atrophy (PRA)
dc.subject.otherretinitis pigmentosa
dc.subject.othercanine
dc.subject.otherdystrophinopathy
dc.subject.otherDuchenne
dc.subject.otherimmunohistochemistry
dc.subject.otherneurometabolic disorder
dc.subject.otherCHILD syndrome
dc.subject.otherILVEN
dc.subject.otherepidermal nevus
dc.subject.otherdiabetes mellitus
dc.subject.otherBurmese cats
dc.subject.othersusceptibility
dc.subject.othersingle-nucleotide polymorphism
dc.subject.othergenetic markers
dc.subject.otherLIPH
dc.subject.otherobesity
dc.subject.othercompanion animals
dc.subject.othermetabolic disease
dc.subject.othercomparative genomics
dc.subject.otherdogs
dc.subject.othercats
dc.subject.otherhorses
dc.subject.othercontactin
dc.subject.otherneurological disorder
dc.subject.otherLeonberger
dc.subject.otherSaint Bernard
dc.subject.otherLabrador retriever
dc.subject.othern/a
dc.titleMolecular Basis of Inherited Diseases in Companion Animals
dc.typebook
oapen.identifier.doi10.3390/books978-3-0365-0473-5
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0
oapen.relation.isbn9783036504728
oapen.relation.isbn9783036504735
oapen.pages232
oapen.place.publicationBasel, Switzerland


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