Gross deletions/duplications inPROS1are relatively common in point mutation-negative hereditary protein S deficiency
Maria C. Pintao, A. A. Garcia, D. Borgel, M. Alhenc-Gelas, C. A. Spek, M. C. H. de Visser, S. Gandrille, Pieter H. ReitsmaVolume:
126
Language:
english
Pages:
8
DOI:
10.1007/s00439-009-0687-9
Date:
September, 2009
File:
PDF, 405 KB
english, 2009