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Native Chemical Ligation at Asx-Cys, Glx-Cys: Chemical Synthesis and High-Resolution X-ray Structure of ShK Toxin by Racemic Protein CrystallographyA Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1A mutation in a rare type of intron in a sodium-channel gene results in aberrant splicing and causes myotonia.Probing α-3(10) transitions in a voltage-sensing S4 helixElucidation of the Covalent and Tertiary Structures of Biologically Active Ts3 Toxin.New mutation of the Na channel in the severe form of potassium-aggravated myotonia.Aberrantly spliced alpha-dystrobrevin alters alpha-syntrophin binding in myotonic dystrophy type 1.Total chemical synthesis of biologically active fluorescent dye-labeled Ts1 toxinA novel mutation in SCN4A causes severe myotonia and school-age-onset paralytic episodes.A case of non-dystrophic myotonia with concomitant mutations in the SCN4A and CLCN1 genes.[A survey of cardiologists, diabetologists, gynecologists and ophthalmologists practicing in Osaka on the medical consultation behaviors of myotonic dystrophy patients]
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P50
description
researcher ORCID ID = 0000-0003-1004-8537
@en
wetenschapper
@nl
name
Tomoya Kubota
@ast
Tomoya Kubota
@en
Tomoya Kubota
@es
Tomoya Kubota
@nl
type
label
Tomoya Kubota
@ast
Tomoya Kubota
@en
Tomoya Kubota
@es
Tomoya Kubota
@nl
prefLabel
Tomoya Kubota
@ast
Tomoya Kubota
@en
Tomoya Kubota
@es
Tomoya Kubota
@nl
P1153
26633163700
P31
P496
0000-0003-1004-8537