Mutation Information
Mutation Site
|
G1899A |
Mutation Type
|
Nucleotide level |
Gene/Protein/Region Type
|
PreC |
Country
|
Japan |
Literature Information
PubMed PMID
|
16871568
|
Disease
|
Acute hepatitis B
|
Published Year
|
2006 |
Journal
|
Hepatology (Baltimore, Md.) |
Title
|
Influence of genotypes and precore mutations on fulminant or chronic outcome of acute hepatitis B virus infection. |
Author
|
Ozasa A,Tanaka Y,Orito E,Sugiyama M,Kang JH,Hige S,Kuramitsu T,Suzuki K,Tanaka E,Okada S,Tokita H,Asahina Y,Inoue K,Kakumu S,Okanoue T,Murawaki Y,Hino K,Onji M,Yatsuhashi H,Sakugawa H,Miyakawa Y,Ueda R,Mizokami M |
Evidence
|
Likewise, mutations in core‐promoter at nt 1753 or nt 1754, and G1899A mutation were more frequent in patients with fulminant than acute hepatitis (P = .0003 and P < .0001, respectively).
|
|
|