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Specific OCRL1 patient mutations differentially impact Lo... | ResearchHub
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Specific OCRL1 patient mutations differentially impact Lowe Syndrome cellular phenotypes
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Authors
Swetha Ramadesikan
11 more
Swetha Ramadesikan
•
Lisette Skiba
9 more
•
R. Aguilar
Published
October 28, 2020
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Preprint Server
Topics
Biology
Pathology
Medicine
Surgery
Cell Biology
Show all topics
DOI
10.1101/2020.08.04.236612
License
cc-no
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Pathology
Medicine
Surgery
Cell Biology
Show all topics
DOI
10.1101/2020.08.04.236612
License
cc-no
