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      G.P.1.05 RYR1 is a common cause of congenital fibre type disproportion with ptosis, ophthalmoplegia, scoliosis and pronounced axial muscle weakness

      Author(s): , , , , , , , ,
      Publication date Created:
      Publication date (Print):
      Journal: Neuromuscular Disorders
      Publisher: Elsevier BV

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          Journal
          Title: Neuromuscular Disorders
          Abbreviated Title: Neuromuscular Disorders
          Publisher: Elsevier BV
          ISSN (Print): 09608966
          Publication date Created: September 2009
          Publication date (Print): September 2009
          Volume: 19
          Issue: 8-9
          Page: 557
          Article
          DOI: 10.1016/j.nmd.2009.06.047
          SO-VID: db8a591f-73fb-422d-962a-8c9e785f2e21
          Copyright © © 2009
          License:

          https://www.elsevier.com/tdm/userlicense/1.0/

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