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  1. Nov 2016
  2. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia
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    1. bandrow 04 Nov 2016
      Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia
      PMID:27392076
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    ncbi.nlm.nih.gov/pmc/articles/PMC5005467/