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Orphanet Journal of Rare Diseases, ISSN 1750-1172, 12/2018, Volume 13, Issue 1, pp. 218 - 218
Journal Article
NeuroMolecular Medicine, ISSN 1535-1084, 3/2012, Volume 14, Issue 1, pp. 40 - 52
In 2002, we identified LMNA as the first gene responsible for an autosomal recessive axonal form of Charcot-Marie-Tooth disease, AR-CMT2A. All patients were... 
Neurosciences | Laminopathy | Lamin A/C | Internal Medicine | Charcot-Marie-Tooth | Knock-in | Neurology | Biomedicine | Mouse | AR-CMT2A | CMT2 | LMNA | PMP22 | Axonal
Journal Article
Neuromolecular Medicine, ISSN 1535-1084, 03/2012, Volume 14, Issue 1, p. 40
In 2002, we identified LMNA as the first gene responsible for an autosomal recessive axonal form of Charcot-Marie-Tooth disease, AR-CMT2A. All patients were... 
Journal Article
Neuromolecular Medicine, ISSN 1535-1084, 03/2012, Volume 14, Issue 1, p. 40
In 2002, we identified LMNA as the first gene responsible for an autosomal recessive axonal form of Charcot-Marie-Tooth disease, AR-CMT2A. All patients were... 
Anopheles | Deregulation | Neurosciences | Developmental biology | Analysis | Genes | Muscles
Journal Article
Neuromolecular Medicine, ISSN 1535-1084, 03/2012, Volume 14, Issue 1, pp. 40 - 52
In 2002, we identified LMNA as the first gene responsible for an autosomal recessive axonal form of Charcot-Marie-Tooth disease, AR-CMT2A. All patients were... 
Animal models | Spinal cord | Molecular modelling | Cardiac muscle | Charcot-Marie-Tooth disease | LMNA protein | Peripheral nerves | Mutation | Peripheral myelin protein 22 | Age | Skeletal muscle
Journal Article
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