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Title
TFG
: At the crossroads of motor neuron disease and myopathy
Authors
Keywords
-
Journal
MUSCLE & NERVE
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2019-09-03
DOI
10.1002/mus.26692
References
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Related references
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- Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
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- (2013) Hong Joo Kim et al. NATURE
- The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement
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- Welander distal myopathy is caused by a mutation in the RNA-binding protein TIA1
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- (2011) Faisal Fecto ARCHIVES OF NEUROLOGY
- Brainstem and spinal cord motor neuron involvement with optineurin inclusions in proximal-dominant hereditary motor and sensory neuropathy
- (2011) K. Fujita et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Autosomal-Dominant Distal Myopathy Associated with a Recurrent Missense Mutation in the Gene Encoding the Nuclear Matrix Protein, Matrin 3
- (2009) Jan Senderek et al. AMERICAN JOURNAL OF HUMAN GENETICS
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