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Sir, The article by Auer-Grumbach et al. (2011) reporting that fibulin 5 (FBLN5) mutations are also linked to inherited neuropathies helped us to clarify the cause of autosomal dominant, demyelinating hereditary motor and sensory neuropathy (HMSN I) in our long-time known, but unsolved, Czech family.
Document: Czech family confirms the link between FBLN5 and Charcot–Marie–Tooth type 1 neuropathy (.pdf; 204 Kb).