Analysis of phenotype and genotype in a Chinese pedigree with inherited prothrombin deficiency resulted from a homozygous mutation Tyr510Asp.
- Author:
Yan-hui JIN
;
Ming-shan WANG
;
Fang-xiu ZHENG
- Publication Type:Journal Article
- MeSH:
Adolescent;
Adult;
Amino Acid Sequence;
Genotype;
Homozygote;
Humans;
Hypoprothrombinemias;
etiology;
genetics;
Male;
Middle Aged;
Molecular Sequence Data;
Mutation;
Pedigree;
Phenotype;
Young Adult
- From:
Chinese Journal of Hematology
2012;33(7):587-589
- CountryChina
- Language:Chinese