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GDAP1 gene

Known as: CMT2K, CMT4, GDAP1 
National Institutes of Health

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GDAP1L1 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
A role for the GDAP 1 gene in the molecular pathogenesis of Charcot ‐ Marie ‐ Tooth disease
In 2002 a series of mutations in the GDAP1 gene were reported in patients suffering from Charcot‐Marie‐Tooth disease manifesting… 
2018
2018
The classification of Charcot-Marie-Tooth diseases, a never-ending story: CMT4?
2017
2017
Similar clinical, pathological, and genetic features in Chinese patients with autosomal recessive and dominant Charcot–Marie–Tooth disease type 2K
2015
2015
P32 - High frequency of SH3TC2 mutations in early-onset CMT4
2015
2015
SPINAL ANESTHESIA IN A PATIENT WITH CHARCOT-MARIE TOOTH DISEASE , WHO UNDERWENT OSTEOSYNTHESIS WITH TIBIA NAIL PLATE
Charcot-Marie Tooth disease (CMT) is a hereditary peripheral neuropathy characterized by muscular atrophy and sensitive… 
Review
2014
Review
2014
Fenótipos Raros de Neuropatia Hereditária: Charcot-Marie-Tooth Tipo 4
Introduction. The Charcot-Marie-Tooth Disease (CMT) comprises a genetic heterogeneous group of motor and sensory inherited… 
2008
2008
シンポジウム11―1 末梢神経障害の研究―最近の進歩― 遺伝性ニューロパチーの病態と治療
Hereditary neuropathies are classified into Charcot-Marie-Tooth disease (CMT), familial amyloid polyneuropathy (FAP), hereditary… 
Review
2008
Review
2008
[Hereditary neuropathy: recent advance].
Hereditary neuropathies are classified into Charcot-Marie-Tooth disease (CMT), familial amyloid polyneuropathy (FAP), hereditary… 
Review
2006
Review
2006
[Molecular genetics of inherited neuropathies].
Inherited neuropathies are clinically and genetically heterogeneous. At least 28 genes and 12 loci have been associated with… 
2003
2003
GDAP1 mutations in CMT4: Axonal and demyelinating phenotypes? The exception “proves the rule”
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