bibliographicCitation |
Burwinkel B, Hu B, Schroers A, Clemens PR, Moses SW, Shin YS, Pongratz D, Vorgerd M, Kilimann MW. Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases. European Journal of Human Genetics. 2003 Jun 27;11(7):516–26. doi: 10.1038/sj.ejhg.5200996. |