Fibrinogen Yecheon: Congenital Dysfibrinogenemia with Gamma Methionine-310 to Threonine Substitution

This case study reports a rare fibrinogen variant, γ Met310Thr mutation, for the first time in Korea. The case shows a point mutation from T to C in the 1,007th nucleotide of the FGG gene. This report describes a variant fibrinogen, hereinafter called "fibrinogen Yecheon", using the name a...

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Detalles Bibliográficos
Autores principales: Park, Eunkyung, Park, Geumbore, Park, Rojin, Kim, Hee-Jin, Lee, Sang Jae, Cha, Young Joo
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2009
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775876/
https://www.ncbi.nlm.nih.gov/pubmed/19949684
http://dx.doi.org/10.3346/jkms.2009.24.6.1203

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775876/
https://www.ncbi.nlm.nih.gov/pubmed/19949684
http://dx.doi.org/10.3346/jkms.2009.24.6.1203

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