A case report of FAVA syndrome in a young woman carrying a mutation in the PIK3CA gene

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
1 Online-Ressource.
Language
Englisch

Bibliographic citation
A case report of FAVA syndrome in a young woman carrying a mutation in the PIK3CA gene ; volume:44 ; number:11 ; day:12 ; month:7 ; year:2023 ; pages:4147-4150 ; date:11.2023
Neurological sciences ; 44, Heft 11 (12.7.2023), 4147-4150, 11.2023

Creator
Costagliola, Antonella
Arcuri, Felice
Pelliccioni, Pietro
Malandrini, Alessandro
De Stefano, Nicola
Battisti, Carla
Contributor
SpringerLink (Online service)

DOI
10.1007/s10072-023-06898-3
URN
urn:nbn:de:101:1-2024010121013047853596
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:20 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Associated

  • Costagliola, Antonella
  • Arcuri, Felice
  • Pelliccioni, Pietro
  • Malandrini, Alessandro
  • De Stefano, Nicola
  • Battisti, Carla
  • SpringerLink (Online service)

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