<scp> <i>SORL1</i> </scp> gene mutation and octapeptide repeat insertion in <scp> <i>PRNP</i> </scp> gene in a case presenting with rapidly progressive dementia and cerebral amyloid angiopathy-Reference-Cited by-同舟云学术

SORL1 gene mutation and octapeptide repeat insertion in PRNP gene in a case presenting with rapidly progressive dementia and cerebral amyloid angiopathy

Published:2022-07-22 Issue:11 Volume:29 Page:3139-3146
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Euro J of Neurology

Author:

Cencini Federica¹^ORCID,Catania Marcella²,Di Fede Giuseppe²,Rossi Giacomina²,Chalouhi Katia Khouri³,Manfredi Chiara¹,Giaccone Giorgio²,Tiraboschi Pietro²,Bersano Anna⁴^ORCID,Groppo Elisabetta¹,Rosci Chiara¹,Tancredi Lucia¹,Campiglio Laura¹,De Grado Amedeo¹,Priori Alberto¹^ORCID,Scelzo Emma¹

Affiliation:

1. I Clinical Neurology Unit, Department of Health Sciences, Aldo Ravelli Research Centre University of Milan, San Paolo University Hospital, ASST Santi Paolo e Carlo Milan Italy

2. Neurology 5/Neuropathology Unit Fondazione IRCCS Istituto Neurologico Carlo Besta Milan Italy

3. Radiology UOC, San Carlo Borromeo Hospital ASST Santi Paolo e Carlo Milan Italy

4. Cerebrovascular Unit Carlo Besta Neurological Institute, Scientific Institute for Research and Health Care Foundation Milan Italy

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.15487

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