Identificación de variantes genéticas en los genes CLCN1 y SCN4A en personas con miotonías hereditarias no distróficas /

Similar Items

• Somatic mosaicism and genotype-phenotype correlations in myotonic dystrophy type 1 /
  by: Morales Montero, Fernando Alberto 1973-
  Published: (2006)
• Distrofia miotónica: una enfermedad hereditaria e incapacitante
  by: Fonseca Calvo, María Eugenia, et al.
• Clinical and molecular diagnosis of a Costa Rica family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCNI gene /
  by: Morales Montero, Fernando Alberto 1973-
• Diagnóstico molecular de la distrofia miotónica en Costa Rica /
  by: Morales Montero, Fernando Alberto 1973-
  Published: (2000)
• Clinical and molecular diagnosis of a Costa Rican family with autosomal resessive mytonia congenita (Becker disease) carrying a new mutation in the CLCN1gene
  by: Morales, Fernando