Novel monoamine oxidase A knock out mice with human-like spontaneous mutation

NeuroReport

Volumn 19, Issue 7, 2008, Pages 739-743

  Scott, Anna L ^a   Bortolato, Marco ^a   Chen, Kevin ^a   Shih, Jean C ^a,b  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

Brunner syndrome; Monoamine oxidase; Nonsense mutation

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME A;

AGGRESSION; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRUNNER SYNDROME; CLINICAL FEATURE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME DEFICIENCY; EXON; GENETIC IDENTIFICATION; INBORN ERROR OF METABOLISM; MOUSE; NONHUMAN; NONSENSE MUTATION; OPEN FIELD BEHAVIOR; PRIORITY JOURNAL; PROTEIN ANALYSIS; SPONTANEOUS MUTATION;

AGGRESSION; ANIMALS; BASE SEQUENCE; DISEASE MODELS, ANIMAL; GENETIC DISEASES, X-LINKED; HUMANS; MALE; MENTAL DISORDERS; MICE; MICE, KNOCKOUT; MOLECULAR SEQUENCE DATA; MONOAMINE OXIDASE; MOTOR ACTIVITY; POINT MUTATION; POLYMERASE CHAIN REACTION;

EID: 42349093469     PISSN: 09594965     EISSN: None     Source Type: Journal    
DOI: 10.1097/WNR.0b013e3282fd6e88     Document Type: Article

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