Autosomal dominant distal myopathy with nemaline rods due to p.Glu197Asp mutation in ACTA1

  1. Hernandez-Lain, A.
  2. Cantero, D.
  3. Camacho-Salas, A.
  4. Toldos, O.
  5. Esteban, I.
  6. Pascual, I.
  7. Dominguez-Gonzalez, C.
Journal:
Neuromuscular Disorders

ISSN: 1873-2364,  0960-8966

Year of publication: 2019

Volume: 29

Issue: 3

Pages: 247-250

Type: Article

DOI: 10.1016/J.NMD.2018.12.001 GOOGLE SCHOLAR
Data source: Scopus