Coding sequence and exon/intron organization of the canine CLN3 (Batten Disease) gene and its exclusion as the locus for ceroid-lipofuscinosis in English setter dogs

Journal of Neuroscience Research

Volumn 52, Issue 3, 1998, Pages 268-275

  Shibuya, Hisashi ^a   Liu, Po Ching ^a   Katz, Martin L ^a,b   Siakotos, Aristotle N ^c   Nonneman, Dan J ^a   Johnson, Gary S ^a  

^a UNIVERSITY OF MISSOURI   (United States)

^b University of Missouri   (United States)

^c INDIANA UNIVERSITY   (United States)

Author keywords

Animal model; Batten disease; CLN3; Gene linkage; Gene sequence; Juvenile ceroid lipofuscinosis

Indexed keywords

COMPLEMENTARY DNA;

AMINO ACID SEQUENCE; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; DOG; EXON; GENE MUTATION; GENETIC LINKAGE; HOMOZYGOSITY; HUMAN; INTRON; LIPOFUSCINOSIS; MARKER GENE; NONHUMAN; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PATHOGENESIS; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; DISEASE MODELS, ANIMAL; DOG DISEASES; DOGS; EXONS; HUMANS; INTRONS; MEMBRANE GLYCOPROTEINS; MICE; MOLECULAR CHAPERONES; MOLECULAR SEQUENCE DATA; MUTATION; NEURONAL CEROID-LIPOFUSCINOSES; PEDIGREE; POLYMERASE CHAIN REACTION; PROTEINS; RABBITS; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 0032080693     PISSN: 03604012     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-4547(19980501)52:3<268::AID-JNR3>3.0.CO;2-B     Document Type: Article

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