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Publications by Naomichi Matsumoto
Corrigendum: Ultra–sensitive Droplet Digital PCR for Detecting a Low–prevalence Somatic GNAQ Mutation in Sturge–Weber Syndrome
Scientific Reports
Multidisciplinary
A novelWDR45mutation in a Patient With Static Encephalopathy of Childhood With Neurodegeneration in Adulthood (SENDA)
American Journal of Medical Genetics, Part A
Genetics
SOFT Syndrome in a Patient From Chile
American Journal of Medical Genetics, Part A
Genetics
Constitutive Activation of mTORC1 Signaling Induced by Biallelic Loss-Of-Function Mutations in SZT2 Underlies a Discernible Neurodevelopmental Disease
PLoS ONE
Multidisciplinary
Characteristics of the Conduction of the Left Atrium in Atrial Fibrillation Using Non-Contact Mapping
Journal of Cardiology
Cardiovascular Medicine
Cardiology
Early-Onset Epileptic Encephalopathy and Severe Developmental Delay in an Association With De Novo Double Mutations in NF1 and MAGEL2
Epilepsia Open
Neurology
Different Types of Suppression-Burst Patterns in Patients With Epilepsy of Infancy With Migrating Focal Seizures (EIMFS)
Seizure : the journal of the British Epilepsy Association
Medicine
Neurology
Intellectual Disability and Dysmorphic Features in Male Siblings Arising From a Novel TAF1 Mutation
Congenital Anomalies
Child Health
Pediatrics
Perinatology
Medicine
Developmental Biology
Embryology
Study on Adsorption Ability of Hydroxyapatite for Strontium in Solutions
Japanese Geotechnical Society Special Publication
Preferential Paternal Origin of Microdeletions Caused by Prezygotic Chromosome or Chromatid Rearrangements in Sotos Syndrome
American Journal of Human Genetics
Genetics
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