Mouse gene knockout models for the CLN2 and CLN3 forms of ceroid lipofuscinosis

European Journal of Paediatric Neurology

Volumn 5, Issue SUPPL. A, 2001, Pages 109-114

  Katz, M L ^a   Johnson, G S ^a  

^a University of Missouri   (United States)

Author keywords

Batten disease; Gene knockout; Lysosomal storage; Mouse models; Neuronal degeneration

Indexed keywords

CLN 2 PROTEIN; CLN 3 PROTEIN; GENE PRODUCT; UNCLASSIFIED DRUG;

ALLELE; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BEHAVIOR DISORDER; BIOACCUMULATION; CHILD; CHILDHOOD DISEASE; CHIMERA; COGNITIVE DEFECT; CONTROLLED STUDY; DEATH; DEGENERATIVE DISEASE; DISEASE CLASSIFICATION; DISEASE SEVERITY; EVALUATION; GENE MUTATION; GENE TARGETING; GENE THERAPY; GENETIC DISORDER; GENETICS; HOMOZYGOSITY; HUMAN; KNOCKOUT MOUSE; LYSOSOME STORAGE DISEASE; MOUSE; NEURONAL CEROID LIPOFUSCINOSIS; NONHUMAN; PATHOLOGY; PREMATURITY; PRIORITY JOURNAL; PROTEIN SYNTHESIS; RETINA DEGENERATION; SCREENING; SEQUENCE HOMOLOGY; SYMPTOM; THERAPY;

EID: 0034916518     PISSN: 10903798     EISSN: None     Source Type: Journal    
DOI: 10.1053/ejpn.2000.0445     Document Type: Article

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