# Myelin protein zero

> mammalian protein found in Homo sapiens

**Wikidata**: [Q14912882](https://www.wikidata.org/wiki/Q14912882)  
**Source**: https://4ort.xyz/entity/myelin-protein-zero-q14912882


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/P25189)
3. Q20641742
4. [Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P25189)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P25189)
6. [De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P25189)
7. [Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P25189)
8. [Different cellular and molecular mechanisms for early and late-onset myelin protein zero mutations](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P25189)
9. [Peripheral myelin modification in CMT1B correlates with MPZ gene mutations](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P25189)
10. Ensembl Release 99