Mutations in KLHL7, a Dominant Retinitis Pigmentosa - Locus, Cause a Recessive Crisponi/CISS1-like phenotype

Références BibTex

@Misc{CAU.CF.16,
  author       = {Crisponi, L. and Angius, A. and Uva, P. and ...,  . and Cuccuru, G. and Fotia, G. and ..., ..},
  title        = {Mutations in KLHL7, a Dominant Retinitis Pigmentosa - Locus, Cause a Recessive Crisponi/CISS1-like phenotype},
  year         = {2016},
  keywords     = {crisponi syndrom, next generation sequencing, exome},
  url          = {https://publications.crs4.it/pubdocs/2016/CAU.CF.16},
}

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