G1896A Precore Mutation and Association With HBeAg Status, Genotype and Clinical Status in Patients With Chronic Hepatitis B | Zendy

Jeyanthi Suppiah | Zendy; Rozainanee Mohd Zain | Zendy; Norazlah Bahari | Zendy; Salbiah Haji Nawi | Zendy; Zainah Saat | Zendy

Open Access

G1896A Precore Mutation and Association With HBeAg Status, Genotype and Clinical Status in Patients With Chronic Hepatitis B

Author(s) -

Jeyanthi Suppiah,

Rozainanee Mohd Zain,

Norazlah Bahari,

Salbiah Haji Nawi,

Zainah Saat

Publication year - 2015

Publication title -

hepatitis monthly

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.264

H-Index - 37

eISSN - 1735-3408

pISSN - 1735-143X

DOI - 10.5812/hepatmon.31490

Subject(s) - medicine , hepatitis b virus , genotype , cirrhosis , asymptomatic carrier , virology , hepatitis b , mutation , population , hbeag , immunology , asymptomatic , virus , gastroenterology , genetics , biology , hbsag , gene , environmental health

Our data suggested an intermediate prevalence of G1896A mutation among Malaysian hepatitis B carriers. The stop codon mutation has a significant association with genotype B and patients with chronic hepatitis B and liver cirrhosis.

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