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Publications by Toshihiro Ohura
HRAS Mutants Identified in Costello Syndrome Patients Can Induce Cellular Senescence: Possible Implications for the Pathogenesis of Costello Syndrome
Journal of Human Genetics
Genetics
Successful Treatment of Cardiac Failure Due to Cardiomyopathy in Propionic Acidemia by Cardiac Resynchronization Therapy and Hemodialysis in a Young Adult
Open Journal of Pediatrics
Three Japanese Patients With Beta-Ketothiolase Deficiency Who Share a Mutation, C.431A>C (H144P) in ACAT1
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Genetic Analysis of Classical 21-Hydroxylase Deficiency Using Polymerase Chain Reaction and Allele-Specific Oligonucleotide Hybridization
Clinical Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
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