Two cases of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P)
Author:
Affiliation:
1. Department of Neurology, National Hospital Organization Toneyama National Hospital
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Reference7 articles.
1. 1) Takashima H, Nakagawa M, Nakahara K, et al. A new type of hereditary motor and sensory neuropathy linked to chromosome 3. Ann Neurol 1997;41:771-780.
2. 2) Ishiura H, Sako W, Yoshida M, et al. The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement. Am J Hum Genet 2012;91:320-329.
3. 3) Fujita K, Yoshida M, Sako W, et al. Brainstem and spinal cord motor neuron involvement with optineurin inclusions in proximal-dominant hereditary motor and sensory neuropathy. J Neurol Neurosurg Psychiatry 2011;82:1402-1403.
4. 5) Maeda K, Kaji R, Yasuno K, et al. Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneity. J Hum Genet 2007;52:907-914.
5. 7) Yagi T, Ito D, Suzuki N. Evidence of TRK-fused gene (TFG1) function in the ubiquitin-proteasome system. Neurobiol Dis 2014;66:83-91.
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Re-survey of 16 Japanese patients with advanced-stage hereditary motor sensory neuropathy with proximal dominant involvement (HMSN-P): Painful muscle cramps for early diagnosis;Intractable & Rare Diseases Research;2023-08-31
2. Sural nerve pathology inTFG‐associated motor neuron disease with sensory neuropathy;Neuropathology;2019-04-08
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