A novel prion protein gene‐truncating mutation causing autonomic neuropathy and diarrhea-Reference-Cited by-同舟云学术

A novel prion protein gene‐truncating mutation causing autonomic neuropathy and diarrhea

Published:2018-07-09 Issue:8 Volume:25 Page:
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Bommarito G.¹^ORCID,Cellerino M.¹,Prada V.¹,Venturi C.¹,Capellari S.²³,Cortelli P.²³^ORCID,Mancardi G. L.¹,Parchi P.³⁴,Schenone A.¹

Affiliation:

1. Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health University of Genoa and Ospedale Policlinico San Martino IRCCS Genoa Italy

2. Dipartimento di Scienze Biomediche e Neuromotorie Università di Bologna Bologna Italy

3. IRCCS Istituto delle Scienze Neurologiche Bologna Italy

4. Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale Università di Bologna Bologna Italy

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.13665

Reference8 articles.

1. A Novel Prion Disease Associated with Diarrhea and Autonomic Neuropathy

2. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

3. Molecular basis of phenotypic variability in sporadc creudeldt-jakob disease

4. Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP

5. Familial prion disease with alzheimer disease-like tau pathology and clinical phenotype

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