A new rare mutation (691delCC/insAAA) in exon 17 of the PYGM gene causing McArdle disease

  1. Quintans, B.
  2. Sanchez-Andrade, A.
  3. Teijeira, S.
  4. Fernandez-Hojas, R.
  5. Rivas, E.
  6. López, M.J.
  7. Navarro, C.
Journal:
Archives of Neurology

ISSN: 0003-9942

Year of publication: 2004

Volume: 61

Issue: 7

Pages: 1108-1110

Type: Article

DOI: 10.1001/ARCHNEUR.61.7.1108 GOOGLE SCHOLAR lock_openOpen access editor

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