Related references
Note: Only part of the references are listed.A hospital based epidemiological study of genetically determined muscle disease in south western Norway
Sylvia Adele Husebye et al.
NEUROMUSCULAR DISORDERS (2020)
Challenges in modelling the Charcot-Marie-Tooth neuropathies for therapy development
Manisha Juneja et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2019)
Estimating prevalence for limb-girdle muscular dystrophy based on public sequencing databases
Wei Liu et al.
GENETICS IN MEDICINE (2019)
Genetic epidemiology, demographic, and clinical characteristics of Charcot-Marie-tooth disease in the island of Gran Canaria (Spain)
Manuel Lousa et al.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM (2019)
Epidemiological study and genetic characterization of inherited muscle diseases in a northern Spanish region
Inmaculada Pagola-Lorz et al.
ORPHANET JOURNAL OF RARE DISEASES (2019)
A Nationwide, Population-Based Prevalence Study of Genetic Muscle Disorders
Alice Theadom et al.
NEUROEPIDEMIOLOGY (2019)
229th ENMC international workshop: Limb girdle muscular dystrophies - Nomenclature and reformed classification Naarden, the Netherlands, 17-19 March 2017
Volker Straub et al.
NEUROMUSCULAR DISORDERS (2018)
A population-based epidemiologic study of adult neuromuscular disease in the Republic of Ireland
Stela Lefter et al.
NEUROLOGY (2017)
Molecular Epidemiology of Charcot-Marie-Tooth Disease in Northern Ostrobothnia, Finland: A Population-Based Study
Maria Marttila et al.
NEUROEPIDEMIOLOGY (2017)
Prevalence of myotonic dystrophy type 1 in adults in western Sweden
Christopher Lindberg et al.
NEUROMUSCULAR DISORDERS (2017)
A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy
John Vissing et al.
BRAIN (2016)
Prevalence study of genetically defined skeletal muscle channelopathies in England
Alejandro Horga et al.
NEUROLOGY (2013)
Charcot-Marie-Tooth disease in Northern England
Charlotte Foley et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2012)
Genetic epidemiology of Charcot-Marie-Tooth in the general population
G. J. Braathen et al.
EUROPEAN JOURNAL OF NEUROLOGY (2011)
Prevalence, mutation spectrum and phenotypic variability in Norwegian patients with Limb Girdle Muscular Dystrophy 2I
Eva Stensland et al.
NEUROMUSCULAR DISORDERS (2011)
Genetic and clinical aspects of Charcot-Marie-Tooth's disease
H. Skre
CLINICAL GENETICS (2010)
Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population
Fiona L. M. Norwood et al.
BRAIN (2009)
High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 21 in Denmark
ML Sveen et al.
ANNALS OF NEUROLOGY (2006)
Novel CLCN1 mutations in Taiwanese patients with myotonia congenita
SB Jou et al.
JOURNAL OF NEUROLOGY (2004)
An epidemiological genetic study of Charcot-Marie-Tooth disease in western Japan
S Kurihara et al.
NEUROEPIDEMIOLOGY (2002)
Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia
C Sun et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2001)
Neuromuscular disorders in childhood: a descriptive epidemiological study from western Sweden
N Darin et al.
NEUROMUSCULAR DISORDERS (2000)