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A homoallelic FECH mutation in a patient with both erythropoietic protoporphyria and palmar keratoderma

✍ Scribed by EI Minder; X Schneider-Yin; R Mamet; L Horev; S Neuenschwander; A Baumer; F Austerlitz; H Puy; N Schoenfeld

No coin nor oath required. For personal study only.

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