§<p>Novel variations, $ Common variations.</p><p>Mutations in Indian patients with fibrinogen deficiency.</p
Though rare in occurrence, patients with rare bleeding disorders (RBDs) are highly heterogeneous and...
<p>Mutations in the gene segments of the six whole genomes of H1N1pdm Indian isolates with respect t...
Congenital afibrinogenemia is characterized by the absence of fibrinogen. Congenital fibrinogen diso...
§<p>Novel variations, $ Common variations.</p><p>Mutations in Indian patients with Factor VII defici...
§<p>Novel variations.</p><p>Mutations in Indian patients with Factor V deficiency.</p
§<p>Novel variations.</p><p>Mutations in Indian patients of Factor X deficiency.</p
§<p>Novel variations.</p><p>Mutations in Indian patients with Factor II deficiency.</p
§<p>Novel variations, $ Common variation.</p><p>Mutations in Indian patients with Bernard Soulier Sy...
§<p>Novel variations.</p><p>All the mutations reported above are reported in <i>F13A</i> gene.</p><p...
Abstract Background Congenital afibrinogenemia (OMIM #202400) is a rare coagulation disorder that wa...
<p>fs. Frameshift mutations; § Novel variations.</p><p>Mutations and polymorphisms in Indian patient...
Objectives: The aim of the study is to identify the underlying mutations of afibrinogenemia and poss...
Introduction: Congenital fibrinogen disorders (CFDs) comprise the quantitative and qualitative fibri...
Fibrinogen is synthesized in hepatocytes in the form of a hexamer composed of two sets of three poly...
Congenital fibrinogen disorders are classified into two types of plasma fibrinogen defects: type I (...
Though rare in occurrence, patients with rare bleeding disorders (RBDs) are highly heterogeneous and...
<p>Mutations in the gene segments of the six whole genomes of H1N1pdm Indian isolates with respect t...
Congenital afibrinogenemia is characterized by the absence of fibrinogen. Congenital fibrinogen diso...
§<p>Novel variations, $ Common variations.</p><p>Mutations in Indian patients with Factor VII defici...
§<p>Novel variations.</p><p>Mutations in Indian patients with Factor V deficiency.</p
§<p>Novel variations.</p><p>Mutations in Indian patients of Factor X deficiency.</p
§<p>Novel variations.</p><p>Mutations in Indian patients with Factor II deficiency.</p
§<p>Novel variations, $ Common variation.</p><p>Mutations in Indian patients with Bernard Soulier Sy...
§<p>Novel variations.</p><p>All the mutations reported above are reported in <i>F13A</i> gene.</p><p...
Abstract Background Congenital afibrinogenemia (OMIM #202400) is a rare coagulation disorder that wa...
<p>fs. Frameshift mutations; § Novel variations.</p><p>Mutations and polymorphisms in Indian patient...
Objectives: The aim of the study is to identify the underlying mutations of afibrinogenemia and poss...
Introduction: Congenital fibrinogen disorders (CFDs) comprise the quantitative and qualitative fibri...
Fibrinogen is synthesized in hepatocytes in the form of a hexamer composed of two sets of three poly...
Congenital fibrinogen disorders are classified into two types of plasma fibrinogen defects: type I (...
Though rare in occurrence, patients with rare bleeding disorders (RBDs) are highly heterogeneous and...
<p>Mutations in the gene segments of the six whole genomes of H1N1pdm Indian isolates with respect t...
Congenital afibrinogenemia is characterized by the absence of fibrinogen. Congenital fibrinogen diso...
DOI
Add to ORKG