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Muscular dystrophy, limb-girdle, type 1A

Known as: Muscular Dystrophy, Limb-Girdle, Type1A, LGMD1A, MUSCULAR DYSTROPHY, PROXIMAL, TYPE 1A 
National Institutes of Health

Related topics

Related topics

7 relations
Autosomal dominant inheritanceContracture of tendo achillesDNAJB6 wt AlleleDysarthria

Broader (1)

Muscular Dystrophies, Limb-Girdle

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2014
Review
2014
Making sense of the muscular dystrophies: Diagnosis and treatment guideline for limb‐girdle muscular dystrophy
The limb-girdle muscular dystrophies (LGMDs) are a heterogeneous group of genetically determined myopathies. In 1954, Walton and… 
2013
2013
Limb Girdle Muscular Dystrophies
Autosomal dominant and recessive limb-girdle muscular dystrophies (LGMD) are a heterogeneous group of genetic diseases with a… 
2009
2009
Myofibrillar myopathy with limb-girdle phenotype in a Thai patient.
Myofibrillar myopathy (MFM) encompasses a genetically and clinically heterogeneous group of inherited or sporadic skeletal muscle… 
2008
2008
Palladin, a novel microfilament protein
Palladin is a novel actin microfilament associated protein, which together with myotilin and myopalladin forms a novel… 
Review
2007
Review
2007
Ins and outs of therapy in limb girdle muscular dystrophies.
2007
2007
Cap disease uncapped
2005
2005
A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21
Correction to: European Journal of Human Genetics (2004) 12, 1033–1040. doi: 10.1038/sj.ejhg.5201289 The authors wish to report… 
1996
1996
Limb-girdle muscular dystrophy: A follow-up study of 79 patients
The limb‐girdle muscular dystrophies (LGMD) are autosomally inherited neuromuscular diseases. Recently six different loci for… 
1995
1995
Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.
Limb-girdle muscular dystrophy (LGMD) is a diagnostic classification encompassing a broad group of proximal myopathies. A gene… 
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