Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome

  1. Campos, Y.
  2. Garcia-Silva, T.
  3. Barrionuevo, C.R.
  4. Cabello, A.
  5. Muley, R.
  6. Arenas, J.
Revue:
Pediatric Neurology

ISSN: 0887-8994

Année de publication: 1995

Volumen: 13

Número: 1

Pages: 69-72

Type: Article

DOI: 10.1016/0887-8994(95)00082-Q GOOGLE SCHOLAR
La source de données: Scopus