Sort   by:  
 Page size 
UnknownClinical, neurophysiological evaluation and genetic features of axonal Charcot-Marie-Tooth disease in a Chinese family.
Not available
S-EPMC10870769 | biostudies-literature
UnknownMitochondria dysfunction in Charcot Marie Tooth 2B Peripheral Sensory Neuropathy
Not available
S-EPMC9293960 | biostudies-literature
UnknownWhole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy.
Not available
S-EPMC4036802 | biostudies-literature
UnknownThe Electrophysiological Features in X-Linked Charcot-Marie-Tooth Disease With Transient Central Nervous System Deficits.
Not available
S-EPMC6036262 | biostudies-literature
UnknownTranscriptional dysregulation by a nucleus-localized aminoacyl-tRNA synthetase associated with Charcot-Marie-Tooth neuropathy.
Not available
S-EPMC6834567 | biostudies-literature
UnknownA novel splicing mutation in 5'UTR of GJB1 causes X-linked Charcot-Marie-tooth disease.
Not available
S-EPMC10009907 | biostudies-literature
Transcriptomicsshoots and roots treated with methotrexate and 5-formyl-thf-Transcriptomic and metabolic changes in Arabidopsis thaliana supplemented with 5-CHO-THF and its relationship with the accumulation and transformation to THF active derivatives
au11-02_cho-thf - shoots and roots treated with methotrexate and 5-formyl-thf - Folates and 1C metabolism - The objective of this study is to investigate the changes on the plant expression profiles due to 5-CHO-THF assimilation and transformation. Additionally, plants supplemented with methotrexate...
ORGANISM(S): Arabidopsis thaliana 
2013-08-01 | E-GEOD-41406 | biostudies-arrayexpress
UnknownMutation Analysis of Gap Junction Protein Beta 1 and Genotype-Phenotype Correlation in X-linked Charcot-Marie-Tooth Disease in Chinese Patients.
Not available
S-EPMC4852665 | biostudies-literature
UnknownImpaired protein translation in Drosophila models for Charcot-Marie-Tooth neuropathy caused by mutant tRNA synthetases.
Not available
S-EPMC4506996 | biostudies-literature
UnknownA recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N).
Not available
S-EPMC3240693 | biostudies-literature
Sort   by:  
 Page size