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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:
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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author Ryu, Sohee
Gu, Ja-Yoon
Hong, Kyung Taek
Han, Doo Hee
Kim, Hyun Kyung
author_facet Ryu, Sohee
Gu, Ja-Yoon
Hong, Kyung Taek
Han, Doo Hee
Kim, Hyun Kyung
author_sort Ryu, Sohee
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spelling pubmed-62405132019-03-01 The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T) Ryu, Sohee Gu, Ja-Yoon Hong, Kyung Taek Han, Doo Hee Kim, Hyun Kyung Ann Lab Med Letter to the Editor The Korean Society for Laboratory Medicine 2019-03 2018-11-13 /pmc/articles/PMC6240513/ /pubmed/30430790 http://dx.doi.org/10.3343/alm.2019.39.2.229 Text en © The Korean Society for Laboratory Medicine http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter to the Editor
Ryu, Sohee
Gu, Ja-Yoon
Hong, Kyung Taek
Han, Doo Hee
Kim, Hyun Kyung
The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T)
title The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T)
title_full The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T)
title_fullStr The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T)
title_full_unstemmed The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T)
title_short The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T)
title_sort first case of congenital prekallikrein deficiency in korea with a novel pathogenic variant (c.1198g>t)
topic Letter to the Editor
url 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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