The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T) | Annals of Laboratory Medicine;: 229-231, 2019. | WPRIM

Main content 1 Search 2 Footer 3

+A A -A High contrast

The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T)

Sohee RYU; Ja-Yoon GU; Kyung-Taek HONG; Doo-Hee HAN; Hyun-Kyung KIM.

Annals of Laboratory Medicine ; : 229-231, 2019.

Article in En | WPRIM | ID: wpr-739107

Responsible library: WPRO

ABSTRACT

ABSTRACT

No abstract available.

Subject(s)

Korea; Prekallikrein

Search on Google

Full text: 1 Index: WPRIM Main subject: Prekallikrein / Korea Country/Region as subject: Asia Language: En Journal: Annals of Laboratory Medicine Year: 2019 Type: Article

Search on Google

Full text: 1 Index: WPRIM Main subject: Prekallikrein / Korea Country/Region as subject: Asia Language: En Journal: Annals of Laboratory Medicine Year: 2019 Type: Article