(Q11690084)
English
Charcot-Marie-Tooth disease type 1C
Charcot-Marie-Tooth disease type 1 that has material basis in heterozygous mutation in the LITAF gene on chromosome 16p13
- CMT slow nerve conduction type C
- CMT1C
- Charcot-Marie-Tooth neuropathy type 1C
- HMSN IC
- HMSN1C
- neuropathy hereditary motor and sensory type 1C
- Charcot-Marie-Tooth Neuropathy, Type 1C
- Cmt, Slow Nerve Conduction Type C
- Charcot-Marie-Tooth disease, demyelinating, Type 1C
- CMT 1C
- Hmsn 1C
- CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C
- Charcot Marie Tooth disease type 1C
- Neuropathy, Hereditary Motor and Sensory, Type 1C
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