Fibrinogen angers with a new deletion (γ GVYYQ 346‐350) causes hypofibrinogenemia with hepatic storage

Introduction: This study reports a family with chronically abnormal blood liver function tests (LFT) and congenital hypofibrinogenemia. The proposita had cirrhosis initially related to alcohol abuse and chronic viral hepatitis C (HCV), but abnormal LFT persisted even when alcohol intake was stopped...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Journal of thrombosis and haemostasis 2007-10, Vol.5 (10), p.1999-2005
Hauptverfasser:	DIB, N., QUELIN, F., TERNISIEN, C., HANSS, M., MICHALAK, S., DE MAZANCOURT, P., ROUSSELET, M. C., CALÈS, P.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Base Sequence Endoplasmic Reticulum, Rough - metabolism Family Health Female Fibrinogen - genetics Fibrinogen - metabolism Fluorescent Antibody Technique, Indirect Gene Deletion hepatic inclusion Hepatitis C - virology Hepatitis C virus Humans hypofibrinogenemia Liver - metabolism Liver Diseases - genetics Liver Diseases - metabolism Liver Function Tests Male Molecular Sequence Data Sequence Analysis, DNA storage liver disease
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!