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MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder)

Known as: MUSCULAR DYSTROPHY, PROXIMAL, TYPE 1B, Muscular Dystrophy, Limb-Girdle, Type 1B, Limb-girdle muscular dystrophy, type 1B 
National Institutes of Health

Related topics

Related topics

5 relations
Autosomal dominant inheritanceBradycardiaCardiomyopathy, DilatedSudden Cardiac Death

Broader (1)

Muscular Dystrophies, Limb-Girdle

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Modeling Cardiomyopathy and Arrhythmias in Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
See Article by El-Battrawy et al Dilated cardiomyopathy (DCM) are genetic heart diseases associated with arrhythmias, which are… 
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… 
2014
2014
G.P.251 The Italian Registry of Limb Girdle Muscular Dystrophy: Natural history, genotype–phenotype correlations and outcome measures
2014
2014
Limb-Girdle Muscular Dystrophy Type 1B
Limb-girdle muscular dystrophy type 1B is characterized by progressive limb-girdle weakness (affecting the pelvic before shoulder… 
2014
2014
G.P.145 LMNA-related muscular dystrophies: Clinical and histopathological spectrum in Argentina
2013
2013
Limb Girdle Muscular Dystrophies
Autosomal dominant and recessive limb-girdle muscular dystrophies (LGMD) are a heterogeneous group of genetic diseases with a… 
2002
2002
Identification of lamin A/C (LMNA) gene mutations in Korean patients with autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy 1B
AbstractMutations in the LMNA gene encoding lamins A and C by alternative splicing have been found to cause at least four… 
Highly Cited
2001
Highly Cited
2001
The role of the nuclear envelope in Emery-Dreifuss muscular dystrophy.
2001
2001
Nuclear envelope abnormalities in fibroblasts of LGMD1B case due to a homozygous nonsense mutation of LMNA gene
1968
1968
Radiation measurements of the effluent from the Phoebus 1B reactor. LA-3787.
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