Population screening for the mutation associated with osteogenesis imperfecta in dachshunds
Author:
Affiliation:
1. Institute for Animal Breeding and Genetics; University of Veterinary Medicine Hannover; Hannover Germany
Publisher
Wiley
Subject
General Veterinary,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1136/vr.101122/fullpdf
Reference17 articles.
1. Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta;BECKER;American Journal of Human Genetics,2011
2. Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta;CABRAL;Nature Genetics,2007
3. Coat variation in the domestic dog is governed by variants in three genes;CADIEU;Science,2009
4. Sequence of normal canine COL1A1 cDNA and identification of a heterozygous a1(I) Collagen Gly208AIa mutation in a severe case of canine osteogenesis imperfecta;CAMPBELL;Archives of Biochemistry and Biophysics,2000
5. Canine COL1A2 mutation resulting in C-terminal truncation of pro-alpha2(I) and severe osteogenesis imperfecta;CAMPBELL;Journal of Bone and Mineral Research,2001
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4. Compound heterozygosity for a frameshift mutation and an upstream deletion that reduces expression of SERPINH1 in siblings with a moderate form of osteogenesis imperfecta;American Journal of Medical Genetics Part A;2019-06-09
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