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.
Zeitschrift:
Clinical Genetics

ISSN: 0009-9163

Datum der Publikation: 2001

Ausgabe: 59

Nummer: 1

Seiten: 48-51

Art: Artikel

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