1个复合杂合突变导致的凝血因子Ⅺ缺陷症家系表型及基因型分析
毕晓洁, 黄道超, 金先富, 姜俊宇, 苏正仙, 陈超超, 沈波
Phenotype and genotype analysis of coagulation factor Ⅺ deficiency caused by a compound heterozygous mutation
BI Xiaojie, HUANG Daochao, JIN Xianfu, JIANG Junyu, SU Zhengxian, CHEN Chaochao, SHEN Bo
检验医学
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2020, (10): 1036
-1039
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DOI: 10.3969/j.issn.1673-8640.2020.10.016
