Two homozygous mutations (R193W and 794/795 delAA) in the myophosphorylase gene in a patient with McArdle's disease.

  1. Martín, M.A.
  2. Rubio, J.C.
  3. Campos, Y.
  4. Vílchez, J.
  5. Cabello, A.
  6. Arenas, J.
Aldizkaria:
Human mutation

ISSN: 1098-1004

Argitalpen urtea: 2000

Alea: 15

Zenbakia: 3

Orrialdeak: 294

Mota: Artikulua

DOI: 10.1002/(SICI)1098-1004(200003)15:3<294::AID-HUMU13>3.0.CO;2-H GOOGLE SCHOLAR
Datuen iturria: Scopus