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Publications by Suneel Kateriya
A Novel LQT-3 Mutation Disrupts an Inactivation Gate Complex With Distinct Rate-Dependent Phenotypic Consequences
Channels
Medicine
Biochemistry
Biophysics
Related publications
Novel Deletion Mutation in the Cardiac Sodium Channel Inactivation Gate Causes Long QT Syndrome
International Journal of Cardiology
Cardiovascular Medicine
Cardiology
KCNJ2 Mutations in Arrhythmia Patients Referred for LQT Testing: A Mutation T305A With Novel Effect on Rectification Properties
Heart Rhythm
Cardiovascular Medicine
Physiology
Cardiology
Deletion of an X-Inactivation Boundary Disrupts Adjacent Gene Silencing
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Identification of a Novel TTC19 Mutation in a Portuguese Family With Complex III Deficiency
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
A Dimeric Hydride-Bridged Complex With Geometrically Distinct Iron Centers Giving Rise to an S = 3 Ground State
MEF2C-related Epilepsy: Delineating the Phenotypic Spectrum From a Novel Mutation and Literature Review
Seizure : the journal of the British Epilepsy Association
Medicine
Neurology
Molecular and Phenotypic Evaluation of a Novel germlineTMEM127mutation With an Uncommon Clinical Presentation
Endocrine-Related Cancer
Cancer Research
Endocrinology
Oncology
Metabolism
Diabetes
Phenotypic Characterization of an Older Adult Male With Late-Onset Epilepsy and a Novel Mutation in ASXL3 Shows Overlap With the Associated Bainbridge-Ropers Syndrome
Neuropsychiatric Disease and Treatment
Marked Intrafamilial Phenotypic Variation in a Family With SOD1 C111Y Mutation
Amyotrophic Lateral Sclerosis
