Document Detail


Population screening for the mutation associated with osteogenesis imperfecta in dachshunds.
MedLine Citation:
PMID:  23315765     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
Osteogenesis imperfecta (OI) is a genetic disorder causing defects in the development of collagen type I. Clinical signs of affected dachshunds include multiple fractures of bones, joint hyperlaxity and dentinogenesis imperfecta. Recently, a recessive mutation in the SERPINH1 gene was detected in dachshunds and enabled the development of a DNA test to identify dachshunds carrying the mutation. The purpose of the present study was to analyse the dachshund breeding population for the frequency of the SERPINH1 mutation among the nine different breed varieties in dachshunds, birth years and countries of origin. We genotyped the OI-associated SERPINH1 mutation in 1352 dachshunds from 12 different European countries including all nine varieties. Genotyping was done using a restriction fragment length polymorphism validated by DNA sequence analysis. The overall frequency of OI carriers was 12.9 per cent. Across all different size varieties, the SERPINH1 mutation was over-represented in wire-haired dachshunds with 17.3 per cent OI carriers. Among the different countries, the proportion of OI carriers was highest in Germany with 20.4 per cent. The test is useful for dachshund breeders to prevent the occurrence of OI-affected dogs and as a diagnostic tool for veterinarians.
Authors:
J Eckardt; S Kluth; C Dierks; U Philipp; O Distl
Related Documents :
23582455 - Functional genomics based understanding of rice endosperm development.
19349645 - Lack of evolutionary conservation at positions important for thermal stability in the y...
1628805 - Genes required for vacuolar acidity in saccharomyces cerevisiae.
22552255 - Retinal function and cfh-arms2 polymorphisms analysis: a pilot study in italian amd pat...
16123235 - What have gonadotrophin overexpressing transgenic mice taught us about gonadal function?
23800505 - Associations of collagen type i α2 polymorphisms with the presence of intracranial ane...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2013-1-12
Journal Detail:
Title:  The Veterinary record     Volume:  -     ISSN:  2042-7670     ISO Abbreviation:  Vet. Rec.     Publication Date:  2013 Jan 
Date Detail:
Created Date:  2013-1-14     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0031164     Medline TA:  Vet Rec     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
Institute for Animal Breeding and Genetics, University of Veterinary Medicine Hannover, Hannover, Germany.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Arsenic and the epigenome: interindividual differences in arsenic metabolism related to distinct pat...
Next Document:  Does oral administration of the amino acid tyrosine affect oestradiol-17? concentration and sexual b...