Phenotypic and genotypic studies of ALS cases in ALS-SMA families-Reference-Cited by-同舟云学术

Phenotypic and genotypic studies of ALS cases in ALS-SMA families

Published:2018-03-01 Issue:5-6 Volume:19 Page:432-437
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Corcia Philippe¹²^ORCID,Vourc’h Patrick²³,Blasco Helene²³,Couratier Philippe⁴,Dangoumau Audrey²,Bellance Remi⁵,Desnuelle Claude⁶,Viader Fausto⁷,Pautot Vivien⁸,Millecamps Stephanie⁹,Bakkouche Salah¹,Salachas FranÇois¹⁰,Andres Christian R.²³,Meininger Vincent¹⁰,Camu William¹¹

Affiliation:

1. Centre SLA, CHU Tours, Tours, France,

2. Department of Neurology, UMR INSERM U930, Université François-Rabelais, Tours, France,

3. Service de Biochimie et Biologie Moléculaire, CHU Tours, Tours, France,

4. Centre SLA, CHU Dupuytren, Limoges, France,

5. Service de Neurologie, CHU Fort de France, Martinique, France,

6. Centre SLA, Hôpital l’Archet, Nice, France,

7. Centre SLA, Service de Neurologie, CHU Caen, Caen, France,

8. Centre SLA, Service de Neurologie, CHU Angers, Angers, France,

9. Centre de Recherche de l’Institut du Cerveau et de la Moelle Epinière, INSERM UMR S975, CNRS UMR7225, Hôpital Pitié-Salpêtrière, Université Pierre et Marie Curie-Paris 6, Paris, France,

10. Fédération des Maladies du Système Nerveux, Centre Référent Maladie Rare SLA, Hôpital de la Pitié-Salpêtrière, Paris, France, and

11. Clinique du Motoneurone, Explorations neurologiques, CHU Gui de Chauliac, Université de Montpellier, Montpellier, France

Publisher

Informa UK Limited

Subject

Clinical Neurology,Neurology

Link

https://www.tandfonline.com/doi/pdf/10.1080/21678421.2018.1440406

Reference19 articles.

1. ALS: Recent Developments from Genetics Studies

2. Spinal muscular atrophy

3. Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis