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Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency
Authors
A. A. Garcia
AC Dykes
+43 more
AM Johansson
B Dahlbäck
B Dahlbäck
B Hurtado
C. A. Spek
CJ Wolf de
CT Esmon
D Borgel
D. Borgel
DA Lane
DK Schmidel
DK Schmidel
E Gómez
E Lanke
H Tatewaki
HK Ploos van Amstel
HK Ploos van Amstel
HS Choung
J Duchemin
J Hoebeeck
JH Yoo
JK Ploos van Amstel
JP Schouten
JT Dunnen den
KE Persson
LFA Maurissen
M. Alhenc-Gelas
M. C. H. de Visser
Maria C. Pintao
MK Kate ten
P García de Frutos
PC Comp
PD Stenson
PH Reitsma
Pieter H. Reitsma
RE Simmonds
S Gandrille
S Gandrille
S. Gandrille
T Yin
U Seligsohn
Y Espinosa-Parrilla
YP Visser de
Publication date
Publisher
'Springer Science and Business Media LLC'
Doi
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Abstract
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Last time updated on 05/06/2019