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fibrinogen gamma- chain
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OMIM - Congenital disorder
OMIM - Unspecified immunity deficiency
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Genetic analysis of a Chinese pedigree affected with Congenital dysfibrinogenemia due to variant of …
A case of inherited afibrinogenemia caused by an IVS7-12A>G splice mutation of FGG gene].
Fibrinogen gamma-chain mutation, p.Ile171His, leads to hereditary hypofibrinogenemia].
Fibrinogen Columbus III: A novel c.963del frameshift mutation in the FGG gene resulting in hypofibri…
Genetic analysis of two Chinese pedigrees affected with Hereditary hypofibrinemia due to missense va…
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The Effects of DLBS1033 on Haemostasis Parameters in Healthy Volunteers
Effect of Urine Alkalinazation on Urinary Inflammatory Markers in Patients With Cystinuria
SNPs in the DNase 1 Gene Impair Its Activity and Are Increased in a STE-ACS Patient Cohort Compared …
Efficacy of Probiotics in the Treatment of Hospitalised Patients With Novel Coronavirus Infection
Panobinostat in Treating Patients With Relapsed or Refractory Acute Lymphoblastic Leukemia or Acute …
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