Is the Next Generation Sequencing the Essential Tool for the Early Diagnostic Approach in Congenital Muscular Dystrophy? New Mutation in the Gen LMNA Associated with Serious Phenotype

  1. Avila, G.
  2. González, A.
  3. Abad, A.
  4. Fournier, B.
  5. León, S.
  6. Corral, J.
  7. Fernández, C.
Revista:
Neurology India

ISSN: 1998-4022 0028-3886

Any de publicació: 2021

Volum: 69

Número: 6

Pàgines: 1835-1837

Tipus: Article

DOI: 10.4103/0028-3886.333448 GOOGLE SCHOLAR