Inherited metabolic disease in companion animals: Searching for nature's mistakes

Veterinary Journal

Volumn 174, Issue 2, 2007, Pages 252-259

  Sewell, Adrian C ^a   Haskins, Mark E ^b   Giger, Urs ^b  

^a UNIVERSITY HOSPITAL FRANKFURT   (Germany)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Companion animals; Diagnostic testing; Inborn errors of metabolism; Inherited diseases; Metabolism

Indexed keywords

CYANOCOBALAMIN; RECOMBINANT ENZYME;

ANIMAL BEHAVIOR; ANIMAL GENETICS; BODY FLUID; CAT DISEASE; CLINICAL FEATURE; DISEASE MODEL; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DOG DISEASE; ENZYME REPLACEMENT; GENE MUTATION; GENETIC DISORDER; HETEROZYGOTE; HUMAN; HUMAN VERSUS ANIMAL COMPARISON; INBORN ERROR OF METABOLISM; LABORATORY TEST; LIPIDOSIS; LYSOSOME STORAGE DISEASE; MALABSORPTION; METABOLITE; MUCOPOLYSACCHARIDOSIS; NONHUMAN; PATHOGENESIS; PET ANIMAL; PROTEOMICS; RADIODIAGNOSIS; REVIEW; SIGNAL TRANSDUCTION; URINALYSIS;

ANIMALS; ANIMALS, DOMESTIC; CAT DISEASES; CATS; DIAGNOSIS, DIFFERENTIAL; DOG DISEASES; DOGS; GENETIC PREDISPOSITION TO DISEASE; METABOLISM, INBORN ERRORS;

ANIMALIA; CANIS FAMILIARIS;

EID: 34548753886     PISSN: 10900233     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tvjl.2006.08.017     Document Type: Review

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