Article

Characterisation of LITAF, a protein associated with Charcot-Marie-Tooth disease type 1C

2018-01-01

Abstract excerpt

Charcot-Marie-Tooth disease (CMT) is the commonest inherited neuromuscular disorder, which affects the peripheral nervous system leading to nerve degeneration. CMT is categorised into two forms, ‘axonal’ and ‘demyelinating’, which reflects the main site of pathology as the axon or Schwann cells respectively. Over 90 genes have been identified associated with the disease. Among the genes associated with demyelinati...

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Literature Corpus work: ac8f2bbf-8b9b-59e8-ae11-f63180e1eb6d
DOI: 10.17863/cam.24036

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