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Dive into the research topics of 'Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome'. Together they form a unique fingerprint.- Sort by
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Shinichi Yotsumoto, T. Hashiguchi, X. Chen, N. Ohtake, A. Tomitaka, H. Akamatsu, K. Matsunaga, S. Shiraishi, H. Miura, J. Adachi, T. Kanzaki
Research output: Contribution to journal › Article › peer-review