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Biallelic loss-of-function OBSCN variants predispose indi... | ResearchHub
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Biallelic loss-of-function OBSCN variants predispose individuals to severe, recurrent rhabdomyolysis
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Authors
Macarena Cabrera‐Serrano
35 more
Macarena Cabrera‐Serrano
•
Laure Caccavelli
33 more
•
Gianina Ravenscroft
Published
June 4, 2021
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Preprint Server
Topics
Biology
Internal Medicine
Medicine
Endocrinology
Genetics And Genomics
Show all topics
DOI
10.1101/2021.06.04.447044
License
cc-no
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Internal Medicine
Medicine
Endocrinology
Genetics And Genomics
Show all topics
DOI
10.1101/2021.06.04.447044
License
cc-no
