2 Matching Annotations
  1. Jul 2018
    1. On 2016 May 30, Heidi Schulz commented:

      According to HGVS guidelines, the p.Q238L mutation described as c.713del15 in the paper, should be named c.713_714+13del. The p.A357V variant mentioned in the paper has a MAF=0.02 in ExAc East Asians and has not been reported in patients with Best disease in the papers cited.


      This comment, imported by Hypothesis from PubMed Commons, is licensed under CC BY.

  2. Feb 2018
    1. On 2016 May 30, Heidi Schulz commented:

      According to HGVS guidelines, the p.Q238L mutation described as c.713del15 in the paper, should be named c.713_714+13del. The p.A357V variant mentioned in the paper has a MAF=0.02 in ExAc East Asians and has not been reported in patients with Best disease in the papers cited.


      This comment, imported by Hypothesis from PubMed Commons, is licensed under CC BY.