Yoshiyuki Furutani

3PUBLICATIONS
19CO-AUTHORS
Gene mappingHaematologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (3)

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|Apr 19, 2024
Identification of Prostaglandin I2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis.

Ayako Chida-Nagai, Hiroyuki Akagawa, Saori Sawai

|Jan 15, 2024
Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia.

Shuhei Morita, Shunsuke Nomura, Kenko Azuma

|Oct 23, 2021
Induced Pluripotent Stem Cell-Derived Cardiomyocytes with SCN5A R1623Q Mutation Associated with Severe Long QT Syndrome in Fetuses and Neonates Recapitulates Pathophysiological Phenotypes.

Emiko Hayama, Yoshiyuki Furutani, Nanako Kawaguchi

Pageof 1

Frequent Collaborators

1 joint publications

Keisuke Okita

1 joint publications

Rumiko Matsuoka

1 joint publications

Shuhei Morita

1 joint publications

Ayako Chida-Nagai

1 joint publications

Hiroyuki Akagawa

1 joint publications

Yue-Jiao Ma

1 joint publications

Satoshi Yakuwa

1 joint publications

Jun Muneuchi

1 joint publications

Kazushi Yasuda

1 joint publications

Hirokuni Yamazawa

Frequent Collaborators

1 joint publications

Keisuke Okita

1 joint publications

Rumiko Matsuoka

1 joint publications

Shuhei Morita

1 joint publications

Ayako Chida-Nagai

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