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Publications by Joy Norris
Revealing the Effects of Missense Mutations Causing Snyder-Robinson Syndrome on the Stability and Dimerization of Spermine Synthase
International Journal of Molecular Sciences
Organic Chemistry
Molecular Biology
Theoretical Chemistry
Inorganic Chemistry
Computer Science Applications
Spectroscopy
Medicine
Catalysis
Physical
Related publications
A Missense Mutation, p.V132G, in the X-Linked Spermine Synthase Gene (SMS) Causes Snyder-Robinson Syndrome
American Journal of Medical Genetics, Part A
Genetics
Polyamine Homeostasis in Snyder-Robinson Syndrome
Medical Sciences
Investigating the Effects of Missense Mutations in MSH2 Gene Associated With Lynch Syndrome
Biophysical Journal
Biophysics
Disease-Causing Missense Mutations in Human DNA Helicase Disorders
Mutation Research - Reviews in Mutation Research
Mutagenesis
Health
Genetics
Toxicology
Analyzing Effects of Naturally Occurring Missense Mutations
Computational and Mathematical Methods in Medicine
Genetics
Molecular Biology
Biochemistry
Applied Mathematics
Microbiology
Simulation
Immunology
Medicine
Modeling
Molecular Effects of Eya1 Domain Mutations Causing Organ Defects in BOR Syndrome
Human Molecular Genetics
Medicine
Genetics
Molecular Biology
Protein Stability and in Vivo Concentration of Missense Mutations in Phenylalanine Hydroxylase
Proteins: Structure, Function and Genetics
Biochemistry
Structural Biology
Molecular Biology
A Novel Missense Mutation (G43S) in the Switch I Region of Rab27A Causing Griscelli Syndrome
Molecular Genetics and Metabolism
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
N8-Acetylspermidine as a Potential Plasma Biomarker for Snyder-Robinson Syndrome Identified by Clinical Metabolomics
Journal of Inherited Metabolic Disease
Genetics
