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.
Revue:
Clinical Genetics

ISSN: 0009-9163

Année de publication: 2001

Volumen: 59

Número: 1

Pages: 48-51

Type: Article

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