3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Related collections

          Author and article information

          Contributors
          (View ORCID Profile)
          Journal
          neurogenetics
          Neurogenetics
          Springer Science and Business Media LLC
          1364-6745
          1364-6753
          January 2020
          October 31 2019
          January 2020
          : 21
          : 1
          : 73-78
          Article
          10.1007/s10048-019-00594-1
          31673878
          5866952d-7e9f-4e13-94f4-08b883a6b0cb
          © 2020

          http://www.springer.com/tdm

          http://www.springer.com/tdm

          History

          Comments

          Comment on this article