Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's disease

  1. Martín, Ma.
  2. Rubio, J.C.
  3. Garcí, A.
  4. Fernández, Ma.F.
  5. Campos, Y.
  6. Krawczak, M.
  7. Cooper, D.N.
  8. Arenas, J.
Aldizkaria:
Clinical Genetics

ISSN: 0009-9163

Argitalpen urtea: 2001

Alea: 59

Zenbakia: 1

Orrialdeak: 48-51

Mota: Artikulua

DOI: 10.1034/J.1399-0004.2001.590108.X GOOGLE SCHOLAR