A deletion in nephronophthisis 4 (NPHP4) is associated with recessive cone-rod dystrophy in standard wire-haired dachshund

Genome Research

Volumn 18, Issue 9, 2008, Pages 1415-1421

  Wiik, Anne Caroline ^a   Wade, Claire ^b,c   Biagi, Tara ^b   Ropstad, Ernst Otto ^a   Bjerkås, Ellen ^a   Lindblad Toh, Kerstin ^b,d   Lingaas, Frode ^a  

^a NORWEGIAN UNIVERSITY OF LIFE SCIENCES   (Norway)

^b BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^c MASSACHUSETTS GENERAL HOSPITAL   (United States)

^d UPPSALA UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

NEPHRORETININ; POLYPEPTIDE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CHROMOSOME 5; CONTROLLED STUDY; DYSTROPHY; EXON; GENE DELETION; GENE LINKAGE DISEQUILIBRIUM; GENOME; INTRON; MEIOSIS; NEPHRONOPHTHISIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RETINA CONE ROD DYSTROPHY; RETINA DEGENERATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE ALIGNMENT; SINGLE NUCLEOTIDE POLYMORPHISM;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; DNA MUTATIONAL ANALYSIS; DOG DISEASES; DOGS; GENE DELETION; GENES, RECESSIVE; MICROSATELLITE REPEATS; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEINS; RETINITIS PIGMENTOSA; SRC HOMOLOGY DOMAINS;

CANIS FAMILIARIS;

EID: 50649097717     PISSN: 10889051     EISSN: 15495469     Source Type: Journal    
DOI: 10.1101/gr.074302.107     Document Type: Article

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