Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutation

  1. Yurrebaso, I.
  2. Casado, O.L.
  3. Barcena, J.
  4. Perez de Nanclares, G.
  5. Aguirre, U.
Aldizkaria:
Neuromuscular Disorders

ISSN: 0960-8966,  1873-2364

Argitalpen urtea: 2014

Alea: 24

Zenbakia: 1

Orrialdeak: 56-62

Mota: Artikulua

DOI: 10.1016/J.NMD.2013.09.005 GOOGLE SCHOLAR

Garapen Iraunkorreko Helburuak

Datuen iturria: Scopus