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Glycine substitution mutations by different amino acids in the same codon of COL7A1 lead to heterogeneous clinical phenotypes of dominant dystrophic epidermolysis bullosa

✍ Scribed by T. Murata; T. Masunaga; H. Shimizu; Y. Takizawa; A Ishiko; N. Hatta; T. Nishikawa

No coin nor oath required. For personal study only.

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