threonine and Andersen Syndrome

threonine has been researched along with Andersen Syndrome 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	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Furukawa, T; Kurokawa, J; Miura, D; Nakamura, K; Ohe, T; Ouchida, M; Shimizu, K; Tani, Y	1

Other Studies

1 other study(ies) available for threonine and Andersen Syndrome

Article	Year
T75M-KCNJ2 mutation causing Andersen-Tawil syndrome enhances inward rectification by changing Mg2+ sensitivity. Journal of molecular and cellular cardiology, 2007, Volume: 43, Issue:2 Topics: Adult; Andersen Syndrome; Base Sequence; Cell Line; Cell Membrane; DNA Mutational Analysis; Female; Genes, Dominant; Humans; Ion Channel Gating; Magnesium; Methionine; Molecular Sequence Data; Mutation; Potassium Channels, Inwardly Rectifying; Protein Transport; Spermine; Threonine	2007

Article

Year

T75M-KCNJ2 mutation causing Andersen-Tawil syndrome enhances inward rectification by changing Mg2+ sensitivity.

Journal of molecular and cellular cardiology, 2007, Volume: 43, Issue:2

Topics: Adult; Andersen Syndrome; Base Sequence; Cell Line; Cell Membrane; DNA Mutational Analysis; Female; Genes, Dominant; Humans; Ion Channel Gating; Magnesium; Methionine; Molecular Sequence Data; Mutation; Potassium Channels, Inwardly Rectifying; Protein Transport; Spermine; Threonine

2007