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  1. Nov 2016
  2. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa
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    1. bandrow 04 Nov 2016
      Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa
      PMID:27392078
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    ncbi.nlm.nih.gov/pmc/articles/PMC5005468/