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Identification of two novel mutations in three children with congenital factor VII deficiency

Liang, KR; Nikuze, L; Zhang, FY; Lu, ZJ; Wei, M; Wei, HY

Wei, HY (corresponding author), Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, 6 Shuangyong Rd, Nanning 530021, Guangxi, Peoples R China.

BLOOD COAGULATION & FIBRINOLYSIS, 2021; 32 (5): 340

Abstract

Congenital factor VII deficiency (FVIID) is a rare F7 gene mutation causing bleeding disorder inherited in an autosomal recessive manner. In this stud......

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