T. Nagai

发表

Isoform-specific mutation in Dystonin-b gene causes late-onset protein aggregate myopathy and cardiomyopathy

Dang M. Tran, Shujiro Okuda, I. Nishino, 2022, bioRxiv.

A point mutation found in the WT1 gene in a sporadic Wilms' tumor without genitourinary abnormalities is identical with the most frequent point mutation in Denys‐Drash syndrome

Y. Akasaka, H. Kikuchi, Junji Hata, 1993, FEBS letters.

Association of Primary Ovarian Insufficiency with a Specific Human Leukocyte Antigen Haplotype (A*24:02-C*03:03-B*35:01) in Japanese Women

T. Ogata, R. Yoshida, Y. Yoshimura, 2011, Sexual Development.

Genomic changes in the WT-gene (WT1) in Wilms' tumors and their correlation with histology.

A. Umezawa, Y. Akasaka, H. Iri, 1992, The American journal of pathology.