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Incomplete penetrance for isolated congenital asplenia in... | ResearchHub
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Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons
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Authors
Alexandre Bolze
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Alexandre Bolze
•
Carlos Rodríguez-Gallego
39 more
•
Jean‐Laurent Casanova
Published
June 27, 2018
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Topics
Biology
Genetics And Genomics
Genetics
Penetrance
Haploinsufficiency
Show all topics
DOI
10.1101/356832
License
CC-BY-NC-ND
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Genetics And Genomics
Genetics
Penetrance
Haploinsufficiency
Show all topics
DOI
10.1101/356832
License
CC-BY-NC-ND
Other Formats
PDF
