Molecular diagnosis of inherited neuromuscular disease

Veterinary Clinics of North America - Small Animal Practice

Volumn 32, Issue 1, 2002, Pages 287-300

  Fyfe, John C ^a  

^a MICHIGAN STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

6 PHOSPHOFRUCTOKINASE; ALPHA LEVO FUCOSIDASE; GLYCOSAMINOGLYCAN;

CAT; CLINICAL FEATURE; DIAGNOSTIC ACCURACY; DIAGNOSTIC PROCEDURE; DIAGNOSTIC TEST; DISEASE MODEL; DOG; FUCOSIDOSIS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC LINKAGE; GENETIC MARKER; GLOBOID CELL LEUKODYSTROPHY; GM1 GANGLIOSIDOSIS; INBORN ERROR OF METABOLISM; MOLECULAR DYNAMICS; MOLECULAR GENETICS; MUCOPOLYSACCHARIDOSIS; MUCOPOLYSACCHARIDOSIS TYPE 7; MUSCULAR DYSTROPHY; MYELIN DEFICIENCY; NARCOLEPSY; NEUROMUSCULAR DISEASE; NONHUMAN; REVIEW; SPECIES DIFFERENCE; THOMSEN DISEASE;

CANIS FAMILIARIS; FELIS CATUS;

EID: 0036142329     PISSN: 01955616     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0195-5616(03)00089-5     Document Type: Review

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