A point mutation (Arg271→Cys) of a homozygote for dysfunctional prothrombin, prothrombin Obihiro, which has a region of high sequence variability
Year: 1995
Type: article
Study design: Case Report
Source: British Journal of Haematology
Authors: TOSHIYDKI MIYATA, YAN‐ZHEN ZHENG, ATSUSHI KATO, HISAO KATO
Institution: Obihiro Kosei General Hospital
Language: English
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W1966156836
