Identification of a unique splice site variant in SLC39A4 in bovine hereditary zinc deficiency, lethal trait A46: An animal model of acrodermatitis enteropathica

Genomics

Volumn 88, Issue 4, 2006, Pages 521-526

  Yuzbasiyan Gurkan, Vilma ^a,b   Bartlett, Elizabeth ^a,c  

^a 2209 Biomedical Physical Sciences ^*  (United States)

^b MICHIGAN STATE UNIVERSITY   (United States)

^c Michigan State University   (United States)

Author keywords

Acrodermatitis enteropathica; Bovine genetics; Bovine hereditary zinc deficiency; Comparative genetics; Exon skipping; Human genetics; Lethal trait A46; Mutation testing; Solute carrier; Splice site mutation; Zinc transport

Indexed keywords

GENE PRODUCT;

ABSORPTION; ACRODERMATITIS ENTEROPATHICA; ANIMAL CELL; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; EMBRYO; EXON; FEMALE; MALE; MUTATION; NONHUMAN; NUCLEOTIDE SEQUENCE; ORTHOLOGY; PRIORITY JOURNAL; RNA SPLICING; ZINC DEFICIENCY;

ACRODERMATITIS; ALTERNATIVE SPLICING; ANIMALS; BIOLOGICAL TRANSPORT; CATION TRANSPORT PROTEINS; CATTLE; CATTLE DISEASES; DEFICIENCY DISEASES; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; EXONS; GENES, LETHAL; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; ZINC;

ANIMALIA; BOS TAURUS;

EID: 33748678900     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/j.ygeno.2006.03.018     Document Type: Article

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