A wide spectrum of Hereditary Motor Sensory Neuropathy (HMSN)
Author:
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Reference9 articles.
1. A new type of hereditary motor and sensory neuropathy linked to chromosome 3
2. Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneity
3. Hereditary motor and sensory neuropathy (proximal dominant form, HMSN-P) among Brazilians of Japanese ancestry
4. Hereditary motor and sensory neuropathy with proximal dominancy in the lower extremities, urinary disturbance, and paroxysmal dry cough
Cited by 4 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. Prevalence and Incidence of Amyotrophic Lateral Sclerosis in Japan;Journal of Epidemiology;2014
3. Neuropathology of proximal-dominant hereditary motor and sensory neuropathy (HMSN-P);Rinsho Shinkeigaku;2013
4. The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement;The American Journal of Human Genetics;2012-08
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