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

Detalles Bibliográficos
Autores principales:	Ryu, Sohee, Gu, Ja-Yoon, Hong, Kyung Taek, Han, Doo Hee, Kim, Hyun Kyung
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Society for Laboratory Medicine 2019
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240513/ https://www.ncbi.nlm.nih.gov/pubmed/30430790 http://dx.doi.org/10.3343/alm.2019.39.2.229

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