MBNL‐dependent impaired development within the neuromuscular system in myotonic dystrophy type 1-Reference-Cited by-同舟云学术

MBNL‐dependent impaired development within the neuromuscular system in myotonic dystrophy type 1

Published:2023-01-17 Issue:1 Volume:49 Page:
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathology Appl Neurobio

Author:

Tahraoui‐Bories Julie¹,Mérien Antoine¹,González‐Barriga Anchel²,Lainé Jeanne²,Leteur Céline³,Polvèche Hélène³,Carteron Alexandre³,De Lamotte Juliette Duchesne⁴,Nicoleau Camille⁴,Polentes Jérome³,Jarrige Margot³,Gomes‐Pereira Mário²,Ventre Erwann⁵,Poydenot Pauline⁵,Furling Denis²,Schaeffer Laurent⁶,Legay Claire⁷,Martinat Cécile¹^ORCID

Affiliation:

1. INSERM/UEVE UMR 861 Université Paris Saclay, I‐STEM Corbeil‐Essonnes France

2. INSERM, Institut de Myologie, Centre de Recherche en Myologie Sorbonne Université Paris France

3. CECS/AFM, I‐STEM Corbeil‐Essonnes France

4. IPSEN Innovation Les Ulis France

5. CYTOO SA, Minatec Grenoble France

6. INMG, INSERM U1217, CNRS UMR5310 Université Lyon 1, Université de Lyon, Hospices Civils de Lyon Lyon France

7. CNRS, SPINN—Saint‐Pères Paris Institute for the Neurosciences Université Paris Cité Paris France

Funder

French Muscular Dystrophy Association

Agence Nationale de la Recherche

Publisher

Wiley

Subject

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

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nan.12876

Reference65 articles.

1. Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene

2. Population Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of State-wide Blood Screening Program

3. Small Molecules Which Improve Pathogenesis of Myotonic Dystrophy Type 1

4. Myotonic dystrophy: approach to therapy

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