Genotype-phenotype correlations of DHP receptor α1-subunit gene mutations causing hypokalemic periodic paralysis

C. Angelini, K. Alderson, R.C. Griggs, R. Tawil, R. Gregg, K. Hogan, P.A. Powers, N. Weinberg, W. Malonee, L.J. Ptáček
  • Neuromuscular Disorders, January 1997, Elsevier
  • DOI: 10.1016/s0960-8966(96)00401-4

The authors haven't finished explaining this publication. If you are the author, sign in to claim or explain your work.

Read Publication

The following have contributed to this page: Prof Corrado Angelini