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TMEM106B and myelination: rare leukodystrophy families reveal unexpected connections
This scientific commentary refers to ‘A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy’, by Simons et al. (doi:10.1093/brain/awx314).
Shranjeno v:
| izdano v: | Brain |
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| Main Authors: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Oxford University Press
2017
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5841148/ https://ncbi.nlm.nih.gov/pubmed/29194508 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awx318 |
| Oznake: |
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