Carnitine palmitoyltransferase 1A deficiency: abnormal muscle biopsy findings in a child presenting with Reye’s syndrome

  1. Bellusci, M.
  2. Quijada-Fraile, P.
  3. Barrio-Carreras, D.
  4. Martin-Hernandez, E.
  5. Garcia-Silva, M.
  6. Merinero, B.
  7. Perez, B.
  8. Hernandez-Lain, A.
Aldizkaria:
Journal of Inherited Metabolic Disease

ISSN: 1573-2665 0141-8955

Argitalpen urtea: 2017

Alea: 40

Zenbakia: 5

Orrialdeak: 751-752

Mota: Artikulua

DOI: 10.1007/S10545-017-0041-7 GOOGLE SCHOLAR