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Genetic and molecular mechanism for distinct clinical phe... | ResearchHub
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Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1
0
Authors
Mao Lin
48 more
Mao Lin
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Mao Lin
46 more
•
Nan Wu
Published
August 8, 2019
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Topics
Biology
Internal Medicine
Medicine
Genetics And Genomics
Genetics
Show all topics
DOI
10.1101/726646
License
CC-BY-NC-ND
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Internal Medicine
Medicine
Genetics And Genomics
Genetics
Show all topics
DOI
10.1101/726646
License
CC-BY-NC-ND
Other Formats
PDF
