Japanese recurrent mutation c.6216+5G>T in COL7A1 leads to a mild phenotype of dystrophic epidermolysis bullosa

Takuji Masunaga, Masataka Saito, Takashi Sasaki, Akiharu Kubo, Masayuki Amagai, Akira Ishiko

Research output: Contribution to journalLetterpeer-review

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