Charcot Marie Tooth disease 2U (CMT2U)
Evidence-based neurology checklist on charcot marie tooth disease 2u (cmt2u): Genetics This is caused by mutations in the MARS gene on chromosome 12q It is late onset age Clinical features Acronym
Genetics
- This is caused by mutations in the MARS gene on chromosome 12q
- It is late onset age
Clinical features
Acronym
References
- Gonzalez M, McLaughlin H, Houlden H, et al; Inherited Neuropathy Consortium. Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2. JNNP 2013; 84:1247-1249.
- Hyun YS, Park HJ, Heo SH, et al. Rare variants in methionyl- and tyrosyl-tRNA synthetase genes in late-onset autosomal dominant Charcot-Marie-Tooth neuropathy. Clin Genet 2014; 86:592-594.
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- Charcot Marie Tooth disease 2A (CMT2A)
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- Charcot Marie Tooth disease 2N (CMT2N)
- Charcot Marie Tooth disease 2O (CMT2O)
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- Charcot Marie Tooth disease 2X (CMT2X)
- Charcot Marie Tooth disease 2Y (CMT2Y)
- Charcot Marie Tooth disease 2Z (CMT2Z)