Comprehensive four-year disease progression assessment of myotonic dystrophy type 1-Reference-Cited by-同舟云学术

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Comprehensive four-year disease progression assessment of myotonic dystrophy type 1

Published:2024-10 Issue: Volume:43 Page:44-52
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

la Fontaine Leandre A^ORCID,Bruijnes Johanna E,Smulders Fran HP,Gorissen-Brouwers Carla,Karnebeek Ilse EA,Braakman Hilde MH,Klinkenberg Sylvia,Mul Karlien,‘t Hoen Peter-Bram AC,van Kuijk Sander MJ,van Engelen Baziel GM,Merkies Ingemar SJ,Faber Catharina G

Funder

Princess Beatrix Foundation for Neuromuscular Diseases

Publisher

Elsevier BV

Reference34 articles.

1. Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program;Johnson;Neurology,2021

2. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3’ end of a transcript encoding a protein kinase family member;Brook;Cell,1992

3. Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classification;De Antonio;Rev Neurol (Paris),2016

4. Myotonic dystrophy;Harper,2009

5. Organ dysfunction and muscular disability in myotonic dystrophy type 1;Kaminsky;Medicine,2011

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