A canine model of cohen syndrome: Trapped neutrophil syndrome

BMC Genomics

Volumn 12, Issue , 2011, Pages

  Shearman, Jeremy R ^a,b   Wilton, Alan N ^a  

^a UNIVERSITY OF NEW SOUTH WALES   (Australia)

^b NATIONAL SCIENCE AND TECHNOLOGY DEVELOPMENT AGENCY   (Thailand)

Author keywords

Cohen syndrome; Dog; Expression; Neutropenia; Trapped neutrophil syndrome; Vesicle protein sorting 13 b; Vesicle transport; VPS13B

Indexed keywords

INTERLEUKIN 8 RECEPTOR; PROTEIN BCL XL; STROMAL CELL DERIVED FACTOR 1; VESICULAR TRANSPORT PROTEIN; VPS13B PROTEIN, HUMAN;

AMINO ACID SEQUENCE; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; COHEN SYNDROME; CONTROLLED STUDY; DOG; EXON; EXPERIMENTAL MODEL; GENE; GENE DELETION; GENE EXPRESSION; GENE LOCATION; GENE MUTATION; GENE SEQUENCE; GENE VPS13B; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC LINKAGE; GENETIC TRANSCRIPTION; LEARNING DISORDER; MENTAL DEFICIENCY; NEUTROPENIA; NONHUMAN; NUCLEOTIDE SEQUENCE; SEQUENCE ANALYSIS; TRAPPED NEUTROPHIL SYNDROME; ANIMAL; ANIMAL DISEASE; CHEMISTRY; CONGENITAL MALFORMATION; DEVELOPMENTAL DISORDER; DISEASE MODEL; DOG DISEASE; FINGER; GENETICS; GENOTYPE; HUMAN; MICROCEPHALY; MOLECULAR GENETICS; MOUSE; MUSCLE HYPOTONIA; MYOPIA; OBESITY; PATHOPHYSIOLOGY; SYNDROME;

ANIMALIA; CANIS FAMILIARIS; MUS;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; DEVELOPMENTAL DISABILITIES; DISEASE MODELS, ANIMAL; DOG DISEASES; DOGS; EXONS; FINGERS; GENETIC LINKAGE; GENOTYPE; HUMANS; MENTAL RETARDATION; MICE; MICROCEPHALY; MOLECULAR SEQUENCE DATA; MUSCLE HYPOTONIA; MYOPIA; NEUTROPENIA; OBESITY; SEQUENCE ANALYSIS; SYNDROME; VESICULAR TRANSPORT PROTEINS;

EID: 79956201848     PISSN: None     EISSN: 14712164     Source Type: Journal    
DOI: 10.1186/1471-2164-12-258     Document Type: Article

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