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.
Zeitschrift:
Neurology India

ISSN: 1998-4022 0028-3886

Datum der Publikation: 2021

Ausgabe: 69

Nummer: 6

Seiten: 1835-1837

Art: Artikel

DOI: 10.4103/0028-3886.333448 GOOGLE SCHOLAR