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CBX1 variants cause a neurodevelopmental syndrome due to ... | ResearchHub
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CBX1 variants cause a neurodevelopmental syndrome due to facultative heterochromatin dysfunction
2
Authors
Yukiko Kuroda
37 more
Yukiko Kuroda
•
Alyssa Rippert
35 more
•
Kosuke Izumi
Published
November 24, 2020
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Preprint Server
Topics
Biology
Genetics And Genomics
Genetics
Chromodomain
Heterochromatin Protein 1
Show all topics
DOI
10.1101/2020.09.29.319228
License
cc-no
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Genetics And Genomics
Genetics
Chromodomain
Heterochromatin Protein 1
Show all topics
DOI
10.1101/2020.09.29.319228
License
cc-no
