Nobutaka Tachibana

2PUBLICATIONS
8CO-AUTHORS
Gene mappingEpigenetics (incl. genome methylation and epigenomics)
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Publications (2)

|Sep 28, 2023
The Structural Abnormalities Are Deeply Involved in the Cause of RPGRIP1-Related Retinal Dystrophy in Japanese Patients.

Kaoruko Torii, Sachiko Nishina, Hazuki Morikawa

|Feb 25, 2022
Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa.

Nobutaka Tachibana, Katsuhiro Hosono, Shuhei Nomura

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Frequent Collaborators

2 joint publications

Yoshihiro Hotta

1 joint publications

Shinji Arai

1 joint publications

Nobuhiko Okamoto

1 joint publications

Kei Mizobuchi