The severity of retinal pathology in homozygous Crb1(rd8/rd8) mice is dependent on additional genetic factors

Understanding phenotype–genotype correlations in retinal degeneration is a major challenge. Mutations in CRB1 lead to a spectrum of autosomal recessive retinal dystrophies with variable phenotypes suggesting the influence of modifying factors. To establish the contribution of the genetic background...

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發表在:Hum Mol Genet
Main Authors: Luhmann, Ulrich F.O., Carvalho, Livia S., Holthaus, Sophia-Martha kleine, Cowing, Jill A., Greenaway, Simon, Chu, Colin J., Herrmann, Philipp, Smith, Alexander J., Munro, Peter M.G., Potter, Paul, Bainbridge, James W.B., Ali, Robin R.
格式: Artigo
語言:Inglês
出版: Oxford University Press 2015
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4262495/
https://ncbi.nlm.nih.gov/pubmed/25147295
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu424
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