Genes
MPZ
OMIMSynonym(s): HMSNIB, CMT1, CMT1B
Locus: 1q22
Protein: Myelin P0 protein
Disorder(s):
- Congenital Hypomyelinating Neuropathy
- Charcot-Marie-Tooth Neuropathy Type 2I/2J
- MPZ-Related Intermediate Charcot-Marie-Tooth Neuropathy
- Roussy-Levy Syndrome
- Charcot-Marie-Tooth Neuropathy Type 1B





