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Publications by Kiyoshi Hayasaka
De Novo Mutations in GNAO1, Encoding a Gαo Subunit of Heterotrimeric G Proteins, Cause Epileptic Encephalopathy
American Journal of Human Genetics
Genetics
A Mutation of COX6A1 Causes a Recessive Axonal or Mixed Form of Charcot-Marie-Tooth Disease
American Journal of Human Genetics
Genetics
Phenotypic Variability in a Family With Townes–Brocks Syndrome
Journal of Human Genetics
Genetics
Unique Food-Entrained Circadian Rhythm in Cysteine414-Alanine Mutant mCRY1 Transgenic Mice
Sleep and Biological Rhythms
Neurology
Physiological Psychology
Neuropsychology
Physiology
Electroweak Physics From Belle
Small Heat Shock Protein 27 Mutation in a Japanese Patient With Distal Hereditary Motor Neuropathy
Journal of Human Genetics
Genetics
The GARS Gene Is Rarely Mutated in Japanese Patients With Charcot–Marie–Tooth Neuropathy
Journal of Human Genetics
Genetics
Nonketotic Hyperglycinemia: Two Patients With Primary Defects of P-Protein and T-Protein, Respectively, in the Glycine Cleavage System
Pediatric Research
Child Health
Pediatrics
Perinatology
Neonatal Hyperbilirubinemia in Japanese Neonates: Analysis of the Heme Oxygenase-1 Gene and Fetal Hemoglobin Composition in Cord Blood
Pediatric Research
Child Health
Pediatrics
Perinatology