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Charcot-Marie-Tooth disease type 1C

MONDO:0010995

Any Charcot-Marie-Tooth disease type 1 in which the cause of the disease is a mutation in the LITAF gene.

Also known as: CMT1C, Charcot-Marie-Tooth disease type 1 caused by mutation in LITAF, Charcot-Marie-Tooth disease, type 1C, HMSN1C, LITAF Charcot-Marie-Tooth disease type 1, CMT 1C, CMT, slow nerve conduction type C, Charcot Marie Tooth disease type 1C

9 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Peripheral nervous system disorder (107) Neuromuscular disease (98) Peripheral neuropathy (90) Charcot-Marie-Tooth disease (43) Human disease (14) Hereditary peripheral neuropathy (6) Hereditary neurological disease (5)
Trials to join now! 7 Not yet recruiting 1 Completed 1
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  • Gene therapy readiness check: new study maps virus immunity in muscle disease patients

    Knowledge-focused Not yet recruiting

    This study will test blood samples from 450 people aged 6 to 60 with inherited neuromuscular diseases to see if they have antibodies that could block gene therapy viruses (AAVs). The goal is to understand how common these antibodies are and which patients might be good candidates…

    Phase: NA • Sponsor: Genethon • Aim: Knowledge-focused

    Last updated Jun 27, 2026 13:04 UTC

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