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In Silico Analysis and In-depth Assessment of a Female Patient with a Missense Mutation in the F12 Gene Associated with Hereditary Angioedema Symptoms: A Case Study

2023-10-04

Abstract excerpt

<title>Abstract</title> <p>Hereditary angioedema (HAE) is a complex genetic disorder characterized by recurrent episodes of localized skin and mucosal swelling, with potential life-threatening complications, particularly in the upper respiratory tract. While much is understood about the mutations behind HAE I-II types, the genetic landscape of type III remains complex. Our study provides a comprehensive explorati...

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Literature Corpus work: 7718d259-5188-5798-b9db-e5e9fb74e882
DOI: 10.21203/rs.3.rs-3382724/v1

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In Silico Analysis and In-depth Assessment of a Female Patient with a Missense Mutation in the F12 Gene Associated with Hereditary Angioedema Symptoms: A Case StudyDOI 10.21203/rs.3.rs-3382724/v1Read

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