Changing Paradigms in Diagnosis of Inherited Defects Associated with Urolithiasis

Veterinary Clinics of North America - Small Animal Practice

Volumn 39, Issue 1, 2009, Pages 111-125

  Bannasch, Danika ^a   Henthorn, Paula S ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Cystine; Cystinuria; Gene; Genetic; Hyperuricosuria; Urate

Indexed keywords

CYSTINE; URATE OXIDASE; URIC ACID;

CHROMOSOME ANALYSIS; CYSTINURIA; DNA SEQUENCE; DOG DISEASE; GENE MAPPING; GENE MUTATION; GENETIC DISORDER; GENETIC PREDISPOSITION; GENETIC SUSCEPTIBILITY; GENOTYPE; HOMOZYGOSITY; HUMAN; HYPERURICOSURIA; INHERITANCE; LIVER METABOLISM; NONHUMAN; PHENOTYPE; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM; URINARY EXCRETION; URINARY TRACT OBSTRUCTION; UROLITHIASIS;

ANIMALS; BREEDING; CYSTINE; DOG DISEASES; DOGS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME; MALE; PURINES; URINARY CALCULI; UROLITHIASIS;

CANIS FAMILIARIS;

EID: 56449116385     PISSN: 01955616     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cvsm.2008.09.006     Document Type: Review

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