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CMT2
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Diverse CMT2 neuropathies are linked to aberrant G3BP interactions in stress granules.
Autophagy and Lysosomal Functionality in CMT2B Fibroblasts Carrying the RAB7K126R Mutation.
A novel IGHMBP2 variant and clinical diversity in Vietnamese SMARD1 and CMT2S patients.
Biallelic variants in MAD2L1BP (p31comet) cause female infertility characterized by oocyte maturatio…
Alteration of the late endocytic pathway in Charcot-Marie-Tooth type 2B disease.
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Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2
Gene Therapy for IGHMBP2-Related Diseases
Research of SORD-CMT Natural History and Epalrestat Treatment
Development of Charcot Marie Tooth Disease (CMT) Pediatric Scale for Children With CMT
Genetics of Charcot-Marie-Tooth Dystrophy and Related Diseases
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