Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.
Bradley, K. J.; Cavaco, B. M.; Bowl, M. R.; Harding, B.; Cranston, T.; Fratter, C.; Besser, G. M.; da Conceição Pereira, M.; Davie, M. W. J.; Dudley, N.; Leite, V.; Sadler, G. P.; Seller, A.; Thakker, R. V.; Clinical Endocrinology, 2006, vol. 64, issue 3, p 299, ISSN 03000664. ISBN 03000664.

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