<i>LMNB1</i>‐duplication mediated nuclear architecture alteration and demyelination of cerebral white matter in a patient with ADLD-Reference-Cited by-同舟云学术

LMNB1‐duplication mediated nuclear architecture alteration and demyelination of cerebral white matter in a patient with ADLD

Published:2024-01-24 Issue:1 Volume:50 Page:
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathology Appl Neurobio

Author:

Roy Vincent¹²,Bienjonetti Isabella¹²,Brodeur Alyssa¹²,Dion‐Albert Laurence¹²,Touzel‐Deschênes Lydia¹²,Gould Peter V.³,Saikali Stephan³,Laforce Robert⁴⁵⁶,Gros‐Louis François¹²^ORCID

Affiliation:

1. Department of Surgery, Faculty of Medicine Université Laval Quebec City Quebec Canada

2. LOEX, Division of Regenerative Medicine CHU de Québec‐Université Laval Research Center Quebec City Quebec Canada

3. Department of Medical Biology, Division of Anatomic Pathology and Neuropathology CHU de Québec Quebec City Quebec Canada

4. Department of Neurological Sciences, Faculty of Medicine Université Laval Quebec City Quebec Canada

5. Division of Neurosciences CHU de Québec‐Université Laval Research Center Quebec City Quebec Canada

6. Clinique Interdisciplinaire de Mémoire CHU de Québec Quebec City Quebec Canada

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nan.12947

Reference17 articles.

2. Autosomal Dominant Leukodystrophy: A Disease of the Nuclear Lamina

3. Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31