Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase beta subunit (PHKB)

Open Access
Authors
  • B. Burwinkel
  • A.J. Maichele
  • O. Aagenaes
  • H.D. Bakker
  • A. Lerner
  • Y.S. Shin
  • J.A. Strachan
  • M.W. Kilimann
Publication date 1997
Journal Human Molecular Genetics
Volume | Issue number 6
Pages (from-to) 1109-1115
Organisations
  • Faculty of Medicine (AMC-UvA)
Document type Article
Note D
Published at https://doi.org/10.1093/hmg/6.7.1109
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