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.
Revista:
Clinical Genetics

ISSN: 0009-9163

Ano de publicación: 2001

Volume: 59

Número: 1

Páxinas: 48-51

Tipo: Artigo

DOI: 10.1034/J.1399-0004.2001.590108.X GOOGLE SCHOLAR
Fonte de datos: Scopus