SOD1-related ALS with anticipation in a large family from Martinique.

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Bibliographic Details
Title: SOD1-related ALS with anticipation in a large family from Martinique.
Authors: Giguet-Valard AG; Neurological and Neuromuscular Rare disorders department, CERCA, University Hospital Center of Martinique, Martinique, France., Bellance R; Neurological and Neuromuscular Rare disorders department, CERCA, University Hospital Center of Martinique, Martinique, France., Jeannin S; Neurological and Neuromuscular Rare disorders department, CERCA, University Hospital Center of Martinique, Martinique, France., Duclos S; Neurological and Neuromuscular Rare disorders department, CERCA, University Hospital Center of Martinique, Martinique, France., Olive P; Neurological and Neuromuscular Rare disorders department, CERCA, University Hospital Center of Martinique, Martinique, France., Allard-Saint-Albin O; Neurological and Neuromuscular Rare disorders department, CERCA, University Hospital Center of Martinique, Martinique, France., Cazeneuve C; University Hospital Center of Paris, La Pitié Salpétrière Hospital, Paris, France., Clot F; University Hospital Center of Paris, La Pitié Salpétrière Hospital, Paris, France., Sophie PV; Genetic Department, University Hospital of Nancy, Hospital of Brabois, Nancy, France., Barnetche T; Rheumatology Department/FHU ACRONIM/Rare Systemic Autoimmune Diseases Reference Center, Bordeaux University, Bordeaux, France., Smith-Ravin J; Research group BIOSPHERES/AREBIO, University of Antilles-Campus Schoelcher, Martinique, France., Goizet C; Department of Medical Genetics, National Reference Center for Rare Diseases 'Neurogenetic', Pellegrin Hospital, Bordeaux University Hospital, Bordeaux, France and.; Rare Diseases Laboratory: Genetics and Metabolism (MRGM), INSERM U1211, Bordeaux University, Bordeaux, France.
Source: Amyotrophic lateral sclerosis & frontotemporal degeneration [Amyotroph Lateral Scler Frontotemporal Degener] 2021 Nov; Vol. 22 (7-8), pp. 545-551. Date of Electronic Publication: 2021 Mar 23.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Taylor & Francis Country of Publication: England NLM ID: 101587185 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2167-9223 (Electronic) Linking ISSN: 21678421 NLM ISO Abbreviation: Amyotroph Lateral Scler Frontotemporal Degener Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2167-9223
DOI:10.1080/21678421.2021.1900870