Evidence of TRK-Fused Gene (TFG1) function in the ubiquitin–proteasome system
A heterozygous mutation in the TRK-Fused Gene (TFG1) has recently been identified in hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P). TFG1 protein is reportedly localized at endoplasmic reticulum (ER) exit sites and modulates ER export, but the mechanism of its ac...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2014-06-01
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Series: | Neurobiology of Disease |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S0969996114000539 |