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Dive into the research topics of 'Japanese recurrent mutation c.6216+5G>T in COL7A1 leads to a mild phenotype of dystrophic epidermolysis bullosa'. Together they form a unique fingerprint.- Sort by
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Takuji Masunaga, Masataka Saito, Takashi Sasaki, Akiharu Kubo, Masayuki Amagai, Akira Ishiko
Research output: Contribution to journal › Letter › peer-review