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The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causi... | ResearchHub
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The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal Community
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Authors
Vandana Jain
5 more
Vandana Jain
•
Venkatesan Radha
3 more
•
Sarah Flanagan
Published
November 27, 2024
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Journal
Clinical Genetics
Topics
Biology
Cancer Oncology
Medicine
Endocrinology, Diabetes And Metabolism
Mutation
Show all topics
DOI
10.1111/cge.14657
License
CC-BY
Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Clinical Genetics
Topics
Biology
Cancer Oncology
Medicine
Endocrinology, Diabetes And Metabolism
Mutation
Show all topics
DOI
10.1111/cge.14657
License
CC-BY
