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Structural studies of KCTD1 and its disease-causing mutan... | ResearchHub
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Structural studies of KCTD1 and its disease-causing mutant P20S provide insights into the protein function and misfunction
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Authors
Nicole Balasco
9 more
Nicole Balasco
•
Alessia Ruggiero
7 more
•
Luigi Vitagliano
Published
June 14, 2024
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Topics
Biology
Biochemistry
Chemistry
Medicine
Internal Medicine
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DOI
10.1101/2024.06.14.599007
License
CC-BY-NC-ND
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PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Biochemistry
Chemistry
Medicine
Internal Medicine
Show all topics
DOI
10.1101/2024.06.14.599007
License
CC-BY-NC-ND
Other Formats
PDF
