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De novo and bi-allelic variants in AP1G1 cause neurodevel... | ResearchHub
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De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy
1
Authors
Muhammad Usmani
35 more
Muhammad Usmani
•
Zubair Ahmed
33 more
•
Saima Riazuddin
Published
July 1, 2021
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Journal
The American Journal of Human Genetics
Topics
Biology
Cell Biology
Genetics
Molecular Biology
Missense Mutation
Show all topics
DOI
10.1016/j.ajhg.2021.05.007
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publisher-specific-oa
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Journal
The American Journal of Human Genetics
Topics
Biology
Cell Biology
Genetics
Molecular Biology
Missense Mutation
Show all topics
DOI
10.1016/j.ajhg.2021.05.007
License
publisher-specific-oa
