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A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function.
- Source :
- Human Molecular Genetics; 1/1/2019, Vol. 28 Issue 1, p124-132, 9p
- Publication Year :
- 2019
Details
- Language :
- English
- ISSN :
- 09646906
- Volume :
- 28
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Human Molecular Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 133646143
- Full Text :
- https://doi.org/10.1093/hmg/ddy336