CMT2A：A Natural History Study of CMT1B
A Natural History Study of CMT1B
ANaturalHistoryStudyofCMT1B,CMT2A,CMT4AandCMT4C·Patienthasoneknowndiseasecausingmutationandonevariantthatislistedasdiseasecausingper ...。其他文章還包含有：「Charcot」、「Charcot-Marie」、「Clinicalandgeneticfeaturesofacohortofpatientswith...」、「CMT2-TypesofCharcot」、「CMT2AGuide:Symptoms」、「CMT2AResearch」、「LamalattiadiCharcot」、「NaturalhistoryofCharcot」
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Charcot
https://charcot-marie-toothnew
CMT2A. CMT2 subtype A (CMT2A) is the most common form of CMT2. It is caused by dominantly inherited mutations in the MFN2 gene, located on ...
Charcot-Marie
https://www.sciencedirect.com
Mutations in the gene encoding MFN2 have been identified as associated with Charcot–Marie–Tooth disease type 2A (CMT2A), a neurological disorder ...
Clinical and genetic features of a cohort of patients with ...
https://www.nature.com
CMT2A was defined as inherited axonal neuropathy with nerve conduction velocities in the upper extremity > 38 m/s associated with MFN2 mutations ...
CMT2 - Types of Charcot
https://www.mda.org
CMT2A is the most common subtype of CMT2 (it accounts for 20% of the cases of axonal CMT) and is caused by defects in the MFN2 gene. The MFN2 gene encodes ...
CMT2A Guide: Symptoms
https://cmtrf.org
CMT2A is caused by mutations in a gene called MFN2, which produces the protein mitofusin-2. As a type 2 CMT, CMT2A is characterized by dysfunction of axons — ...
CMT2A Research
https://www.cmtausa.org
Learn about CMT2A research projects the CMTA is funding and learn more about how we collaborate with STAR Biotech Alliance Partners.
La malattia di Charcot
https://www.centrodinoferrari.
La CMT2A è una malattia ad ereditarietà autosomica dominante caratterizzata da progressiva debolezza muscolare, associata ad atrofia, perdita di sensibilità e ...
Natural history of Charcot
https://www.ncbi.nlm.nih.gov
CMT2A is a progressive disease with regards to length-dependent weakness and sensory loss and a cross-sectional analysis of the baseline data of ...