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A point mutation in ABC1 gene in a patient with a severe premature chd and a mild phenotype of tangier disease

✍ Scribed by Bertolini, S.; Pisciotta, L.; Seri, M.; Cusano, R.; Cantafora, A.; Calabresi, L.; Franceschini, G.; Ravazzolo, R.; Calandra, S.

No coin nor oath required. For personal study only.

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