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t/gene-fgg

FGG gene

Discuss publications and research concerning the FGG gene.

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Single Nucleotide Polymorphisms in Distant Kinship Inference and Forensic Genetic Genealogy.
FGG
Genetic mutations associated with congenital fibrinogen disorders: global distribution and clinical outcomes.
FGG
Clinical and patient-reported outcomes of periodontal phenotype modification therapy using injectable platelet rich fibrin with microneedling and free gingival grafts: A prospective clinical trial.
FGG
[Analysis of two pedigrees affected with inherited dysfibrinogenemia due to a novel c.1115 T>A variant of the FGB gene].
FGG
Molecular dynamics-based analyses of the structural instability and secondary structure of the fibrinogen gamma chain protein with the D356V mutation.
FGG
Two symptomatic cases of dysfibrinogenemia in China: one with gamma-chain Arg275Cys mutation and another without detectable mutation in fibrinogen genes.
FGG
The contribution of genetic and environmental factors to changes in total and γ' fibrinogen over 5 years.
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A novel fibrinogen γ chain frameshift deletion (c.637delT) in a patient with hypodysfibrinogenemia associated with thrombosis.
FGG
A novel fibrinogen mutation (γ Thr277Arg) causes hereditary hypofibrinogenemia in a Chinese family.
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Congenital fibrinogen disorders: an update.
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