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A novel mutation in the N-terminal region of theCYP17A1gene in a patient with 17α-hydroxylase/17,20-lyase deficiency

✍ Scribed by Nuzzo, V.; Tauchmanova, L.; Brunetti-Pierri, R.; Zuccoli, A.; Lupoli, G.; Colao, A.; Brunetti-Pierri, N.

No coin nor oath required. For personal study only.

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