|
Mutation Information
|
Mutation Site
|
L49R |
|
Mutation Type
|
Amino acid level |
|
Gene/Protein/Region Type
|
S |
|
Genotype/Subtype
|
D |
|
Country
|
Germany |
Literature Information
|
PubMed PMID
|
30229977
|
|
Disease
|
Acute on chronic liver failure
|
|
Published Year
|
2019 |
|
Journal
|
Hepatology (Baltimore, Md.) |
|
Title
|
Clinical Outcome and Viral Genome Variability of Hepatitis B Virus-Induced Acute Liver Failure. |
|
Author
|
Anastasiou OE,Widera M,Westhaus S,Timmer L,Korth J,Gerken G,Canbay A,Todt D,Steinmann E,Schwarz T,Timm J,Verheyen J,Ciesek S |
|
Evidence
|
Amino acid deletions (del; 16-22 and 20-22) in preS2 and SHB mutation L49R were exclusively detected in patients with ALF-NSR.
|
|
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HBV Mutation Detail Information