valine and Eulenburg Disease

valine has been researched along with Eulenburg Disease in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Feng, Y; Ji, X; Sun, X; Wang, H; Zhang, C	1

Other Studies

1 other study(ies) available for valine and Eulenburg Disease

Article	Year
Severe phenotypes of paralysis periodica paramyotonia are associated with the Met1592Val mutation in the voltage-gated sodium channel gene (SCN4A) in a Chinese family. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2011, Volume: 18, Issue:8 Topics: China; DNA Mutational Analysis; Electromyography; Family Health; Genetic Predisposition to Disease; Humans; Methionine; Muscle, Skeletal; Mutation; Myotonic Disorders; NAV1.4 Voltage-Gated Sodium Channel; Neural Conduction; Phenotype; Sodium Channels; Valine	2011

Article

Year

Severe phenotypes of paralysis periodica paramyotonia are associated with the Met1592Val mutation in the voltage-gated sodium channel gene (SCN4A) in a Chinese family.

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2011, Volume: 18, Issue:8

Topics: China; DNA Mutational Analysis; Electromyography; Family Health; Genetic Predisposition to Disease; Humans; Methionine; Muscle, Skeletal; Mutation; Myotonic Disorders; NAV1.4 Voltage-Gated Sodium Channel; Neural Conduction; Phenotype; Sodium Channels; Valine

2011