Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency

por Pintao, Maria C., Garcia, A. A., Borgel, D., Alhenc-Gelas, M., Spek, C. A., de Visser, M. C. H., Gandrille, S., Reitsma, Pieter H.
Publicado 2009