Your browser doesn't support javascript.
loading
Corrigendum: Case report: De novo mutation of a-galactosidase A in a female patient with end-stage renal disease: report of a case of late diagnosis of Anderson-Fabry disease.
Simonetta, Irene; Riolo, Renata; Todaro, Federica; Donadio, Vincenzo; Incensi, Alex; Miceli, Salvatore; Colomba, Paolo; Duro, Giovanni; Tuttolomondo, Antonino.
Afiliación
  • Simonetta I; Internal Medicine and Stroke Care Ward, Regional Reference Center for Diagnosis and Treatment of Anderson-Fabry Disease, Department of Health Promotion, Maternal and Child Health, Internal Medicine and Specialty Excellence "G. D'Alessandro" (PROMISE), University of Palermo, Palermo, Italy.
  • Riolo R; Internal Medicine and Stroke Care Ward, Regional Reference Center for Diagnosis and Treatment of Anderson-Fabry Disease, Department of Health Promotion, Maternal and Child Health, Internal Medicine and Specialty Excellence "G. D'Alessandro" (PROMISE), University of Palermo, Palermo, Italy.
  • Todaro F; Internal Medicine and Stroke Care Ward, Regional Reference Center for Diagnosis and Treatment of Anderson-Fabry Disease, Department of Health Promotion, Maternal and Child Health, Internal Medicine and Specialty Excellence "G. D'Alessandro" (PROMISE), University of Palermo, Palermo, Italy.
  • Donadio V; Neuromuscular and Neuroimmunology Unit, Bellaria Hospital, IRCCS Institute of Neurological Sciences of Bologna, Bologna, Italy.
  • Incensi A; Neuromuscular and Neuroimmunology Unit, Bellaria Hospital, IRCCS Institute of Neurological Sciences of Bologna, Bologna, Italy.
  • Miceli S; Internal Medicine and Stroke Care Ward, Regional Reference Center for Diagnosis and Treatment of Anderson-Fabry Disease, Department of Health Promotion, Maternal and Child Health, Internal Medicine and Specialty Excellence "G. D'Alessandro" (PROMISE), University of Palermo, Palermo, Italy.
  • Colomba P; Institute for Biomedical Research and Innovation (IRIB-CNR), National Research Council of Italy, Palermo, Italy.
  • Duro G; Institute for Biomedical Research and Innovation (IRIB-CNR), National Research Council of Italy, Palermo, Italy.
  • Tuttolomondo A; Internal Medicine and Stroke Care Ward, Regional Reference Center for Diagnosis and Treatment of Anderson-Fabry Disease, Department of Health Promotion, Maternal and Child Health, Internal Medicine and Specialty Excellence "G. D'Alessandro" (PROMISE), University of Palermo, Palermo, Italy.
Front Genet ; 15: 1368953, 2024.
Article en En | MEDLINE | ID: mdl-38425717
ABSTRACT
[This corrects the article DOI 10.3389/fgene.2023.1122893.].
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Genet Año: 2024 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Genet Año: 2024 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza