(Q70656696)
Statements
Glanzmann's thrombasthenia caused by homozygosity for a splice defect that leads to deletion of the first coding exon of the glycoprotein IIIa mRNA (English)
Simsek S
Heyboer H
de Bruijne-Admiraal LG
Goldschmeding R
Cuijpers HT
von dem Borne AE