Abstract
This scientific commentary refers to ‘A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy’, by Simons et al. (doi:10.1093/brain/awx314).
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Comment
MeSH terms
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Frontotemporal Lobar Degeneration*
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Humans
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Membrane Proteins / genetics
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Mutation
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Nerve Tissue Proteins / genetics*
Substances
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Membrane Proteins
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Nerve Tissue Proteins
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TMEM106B protein, human