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A Japanese-specific recurrent mutation and a novel splice site mutation in the LAMC2 gene identified in two Japanese families with Herlitz junctional epidermolysis bullosa

✍ Scribed by M. Kouno; R. Ko; A. Shimizu; T. Ouchi; K. Sueoka; T. Masunaga; A. Ishiko

No coin nor oath required. For personal study only.

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