Canine Chondrodysplasia Caused by a Truncating Mutation in Collagen-Binding Integrin Alpha Subunit 10

PLoS ONE

Volumn 8, Issue 9, 2013, Pages

  Kyöstilä, Kaisa ^a,b   Lappalainen, Anu K ^a   Lohi, Hannes ^a,b  

^a UNIVERSITY OF HELSINKI   (Finland)

^b FOLKHÄLSAN INSTITUTE OF GENETICS   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA INTEGRIN; ALPHA10 INTEGRIN; ARGININE; COLLAGEN BINDING PROTEIN; CYTOSINE; INTEGRIN RECEPTOR; THYMINE; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BONE GROWTH; BREED DIFFERENCE; CARTILAGE CELL; CHONDRODYSPLASIA; CHROMOSOME 17; CONTROLLED STUDY; DISEASE SEVERITY; DWARFISM; ENCHONDRAL OSSIFICATION; EXON; FEMALE; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE PRODUCT; GENE SEGREGATION; GENETIC ASSOCIATION; HETEROZYGOSITY; ITGA10 GENE; MALE; MOLECULAR GENETICS; MUTATIONAL ANALYSIS; NONHUMAN; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PHENOTYPE; PROTEIN EXPRESSION; SHORT STATURE;

ANIMALS; BONE AND BONES; BONE DISEASES, DEVELOPMENTAL; CARTILAGE; CHONDROCYTES; CHROMOSOMES, MAMMALIAN; CODON, NONSENSE; COLLAGEN; DOGS; EXONS; GENETIC TESTING; HUMANS; INTEGRIN ALPHA CHAINS; PEDIGREE; PROTEIN BINDING;

EID: 84884567163     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0075621     Document Type: Article

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