Mutations in the COL18A1 gen associated with knobloch syndrome and structural brain anomalies: a novel case report and literature review of neuroimaging findings

  1. Irene Díez García-Prieto, I.
  2. Lopez-Martín, S.
  3. Albert, J.
  4. Jiménez de la Peña, M.
  5. Fernández-Mayoralas, D.M.
  6. Calleja-Pérez, B.
  7. Gómez Fernández, M.T.
  8. Álvarez, S.
  9. Pihlajaniemi, T.
  10. Izzi, V.
  11. Fernández-Jaén, A.
Aldizkaria:
Neurocase

ISSN: 1465-3656,  1355-4794

Argitalpen urtea: 2022

Alea: 28

Zenbakia: 1

Orrialdeak: 11-18

Mota: Artikulua

DOI: 10.1080/13554794.2021.1928228 GOOGLE SCHOLAR lock_openSarbide irekia editor
Datuen iturria: Scopus