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Exome sequencing identifies NBEAL2 as the causative gene ... | ResearchHub
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Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome
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Authors
Cornelis Albers
19 more
Cornelis Albers
•
Ana Cvejic
17 more
•
Willem Ouwehand
Published
July 17, 2011
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Journal
Nature Genetics
Topics
Biology
Bioinformatics
Immunology
Hematology
Cardiology And Cardiovascular Medicine
Show all topics
DOI
10.1038/ng.885
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Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Nature Genetics
Topics
Biology
Bioinformatics
Immunology
Hematology
Cardiology And Cardiovascular Medicine
Show all topics
DOI
10.1038/ng.885
Other Formats
PDF
