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Neurology, ISSN 0028-3878, 03/2018, Volume 90, Issue 10, pp. 445 - 446
The evolution of the inherited neuropathy nomenclatures reflects each era's technology. We enter the molecular era and the promise of precision individualized... 
SENSORY NEURON DISEASES | LOWER MOTOR | PERONEAL MUSCULAR-ATROPHY | MUTATIONS | CLINICAL NEUROLOGY | ELECTROPHYSIOLOGIC FINDINGS
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 09/1996, Volume 5, Issue 9, pp. 1377 - 1382
Journal Article
ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 08/2019, Volume 14, Issue 1, pp. 197 - 11
Background Charcot-Marie-Tooth (CMT) disease is the most common inherited neuromuscular disorder characterized by wide clinical, genetic and pathomechanistic... 
MEDICINE, RESEARCH & EXPERIMENTAL | Novel | SERVER | DISEASE | MOTOR | GENETICS & HEREDITY | FRAMEWORK | Cluster | PMP2 | CMT | PERONEAL MUSCULAR-ATROPHY | Demyelinating | Crystals | Amino acids | Family | Genetic aspects | Structure | Fatty acids | Neurophysiology
Journal Article
Neurology, ISSN 0028-3878, 03/2018, Volume 90, Issue 10, pp. e870 - e876
Journal Article
HUMAN MOLECULAR GENETICS, ISSN 0964-6906, 10/2013, Volume 22, Issue 20, pp. 4224 - 4232
CharcotMarieTooth disease (CMT) comprises a clinically and genetically heterogeneous group of peripheral neuropathies characterized by progressive distal... 
EXCHANGE FACTOR | RHOA GEF | MYELIN | PERIPHERAL-NERVES | GENE | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | MARIE-TOOTH DISEASE | NEUROPATHIES | PERONEAL MUSCULAR-ATROPHY | SCHWANN-CELLS | NF-KAPPA-B
Journal Article
Biomaterials, ISSN 0142-9612, 2008, Volume 30, Issue 3, pp. 363 - 373
Journal Article