Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients.
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Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients.
description
2016 nî lūn-bûn
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2016年の論文
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name
Whole-exome sequencing to iden ...... severe hemophilia A patients.
@en
Whole-exome sequencing to iden ...... severe hemophilia A patients.
@nl
type
label
Whole-exome sequencing to iden ...... severe hemophilia A patients.
@en
Whole-exome sequencing to iden ...... severe hemophilia A patients.
@nl
prefLabel
Whole-exome sequencing to iden ...... severe hemophilia A patients.
@en
Whole-exome sequencing to iden ...... severe hemophilia A patients.
@nl
P50
P1433
P1476
Whole-exome sequencing to iden ...... severe hemophilia A patients.
@en
P2093
Elena Santagostino
Maria Rosaria Fasulo
P304
P356
10.1182/BLOOD-2015-12-685735
P407
P50
P577
2016-04-08T00:00:00Z