Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7-Reference-Cited by-同舟云学术

Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7

Published:2021-02-17 Issue:7 Volume:36 Page:1664-1675
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Estiar Mehrdad A.¹²,Yu Eric¹²,Haj Salem Ikhlass³,Ross Jay P.¹²,Mufti Kheireddin¹²,Akçimen Fulya¹²,Leveille Etienne⁴,Spiegelman Dan²,Ruskey Jennifer A.²,Asayesh Farnaz²,Dagher Alain²,Yoon Grace⁵,Tarnopolsky Mark⁶,Boycott Kym M.⁷,Dupre Nicolas⁸⁹,Dion Patrick A.¹²¹⁰,Suchowersky Oksana¹¹,Trempe Jean‐Francois¹²¹³,Rouleau Guy A.¹²¹⁰^ORCID,Gan‐Or Ziv¹²¹⁰^ORCID

Affiliation:

1. Department of Human Genetics McGill University Montréal Québec Canada

2. The Neuro (Montreal Neurological Institute‐Hospital) McGill University Montréal Québec Canada

3. Faculté de Médecine Université Laval Quebec City Québec Canada

4. Faculty of Medicine McGill University Montréal Québec Canada

5. Divisions of Neurology and Clinical and Metabolic Genetics, Department of Paediatrics University of Toronto Toronto Ontario Canada

6. Department of Pediatrics McMaster University Hamilton Ontario Canada

7. Children's Hospital of Eastern Ontario Research Institute University of Ottawa Ottawa Ontario Canada

8. Neuroscience Axis, CHU de Québec Université Laval Québec City Québec Canada

9. Department of Medicine, Faculty of Medicine Université Laval Québec City Québec Canada

10. Department of Neurology and Neurosurgery McGill University Montréal Québec Canada

11. Departments of Medicine (Neurology) and Medical Genetics University of Alberta Edmonton Alberta Canada

12. Department of Pharmacology & Therapeutics McGill University Montréal Québec Canada

13. Centre de Recherche en Biologie Structurale McGill University Montréal Québec Canada

Funder

Canadian Institutes of Health Research

Faculty of Medicine, McGill University

Fonds de Recherche du Québec - Santé

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28528

Reference67 articles.

1. PNPLA6 mutations cause Boucher-Neuhäuser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum

2. A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia

3. Triple A syndrome presenting as complicated hereditary spastic paraplegia

4. Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes

5. Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy

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