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Takuya Naruto

Tokyo Medical and Dental University
University of Tokushima

65

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488

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Somatic mutation in RUNX1 underlies mucocutaneus inflammatory manifestations.

2021 Rheumatology
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The Benefits and Respective Side-Effects of PE Therapy for Intractable Kawasaki Disease

2021 Journal of Clinical Medicine
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APRIL-dependent life-long plasmacyte maintenance and immunoglobulin production in humans.

2020 The Journal of Allergy and Clinical Immunology
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Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome

2020 American Journal of Medical Genetics Part A
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Whole-Exome Sequencing-Based Approach for Germline Mutations in Patients with Inborn Errors of Immunity.

2020 Journal of Clinical Immunology
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Tatton-Brown-Rahman syndrome with a novel DNMT3A mutation presented severe intellectual disability and autism spectrum disorder.

2020 Human genome variation
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Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations.

2020 International Immunology
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Novel compound heterozygous CDH23 variants in a patient with Usher syndrome type I

2019 Human genome variation
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Association of Germline Variants of TCF3 and PAX5 with Pediatric Acute Lymphoblastic Leukemia Development

2019 Blood
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A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM)

2019 Clinical Immunology
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