TMEM106B and myelination: rare leukodystrophy families reveal unexpected connections.
editorial · Level V
Where this comes from
- Record sourced from PubMed, PMID 29194508.
- Also identified by DOI 10.1093/brain/awx318 and PMC identifier 5841148.
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Abstract
<b>This scientific commentary refers to ‘A recurrent <i>de novo</i> mutation in <i>TMEM106B</i> causes hypomyelinating leukodystrophy’, by Simons <i>et al.</i> (doi:10.1093/brain/awx314)</b>.
Medical subject headings
- Frontotemporal Lobar Degeneration
- Nerve Tissue Proteins