A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle's disease

  1. Martín, M.A.
  2. Rubio, J.C.
  3. Campos, Y.
  4. Ricoy, J.R.
  5. Cabello, A.
  6. Arenas, J.
Journal:
Neuromuscular Disorders

ISSN: 0960-8966

Year of publication: 2000

Volume: 10

Issue: 6

Pages: 447-449

Type: Article

DOI: 10.1016/S0960-8966(99)00124-8 GOOGLE SCHOLAR
Data source: Scopus