Inherited motor-sensory neuropathy with upper limb predominance associated with the tropomyosin-receptor kinase fused gene-Reference-Cited by-同舟云学术

Inherited motor-sensory neuropathy with upper limb predominance associated with the tropomyosin-receptor kinase fused gene

Published:2020-03 Issue:3 Volume:30 Page:227-231
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Fabrizi Gian Maria^ORCID,Høyer Helle,Taioli Federica,Cavallaro Tiziana,Hilmarsen Hilde Tveitan,Squintani Giovanna Maddalena,Zanette Giampietro,Braathen Geir Julius

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference20 articles.

1. Mechanisms by which TFG functions in protein secretion and oncogenesis;Witte;Nat Cell Biol,2011

2. The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement;Ishiura;Am J Hum Genet,2012

3. Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene;Lee;JAMA Neurol,2013

4. HMSN-P caused by p.Pro285Leu mutation in TFG is not confined to patients with Far East ancestry;Alavi;Neurobiol Aging,2015

5. Sural nerve pathology in TFG-associated motor neuron disease with sensory neuropathy;Li;Neuropathology,2019

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1. Hereditary motor sensory neuropathy with proximal involvement (HMSN‐P) associated with TFG p.Pro285Leu variant in an Italian family with a motor neuron disease‐like clinical picture;Muscle & Nerve;2024-03-27

2. The Therapeutic Potential of Vitamins B1, B3 and B6 in Charcot–Marie–Tooth Disease with the Compromised Status of Vitamin-Dependent Processes;Biology;2023-06-22

3. A novel TFG c.793C>G mutation in a Chinese pedigree with Charcot‐Marie‐Tooth disease 2;Brain and Behavior;2020-07-14