Pages that link to "Q24319923"

The following pages link to Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretion (Q24319923):

Displaying 7 items.

• Fibrinogen beta chain (Q21137060) (← links)
• Fibrinogen alpha chain (Q21151082) (← links)
• Fibrinogen gamma chain (Q21172240) (← links)
• The natural occurrence of human fibrinogen variants disrupting inter-chain disulfide bonds (A Cys36Gly, A Cys36Arg and A Cys45Tyr) confirms the role of N-terminal A disulfide bonds in protein assembly and secretion (Q35143518) (← links)
• A Novel Mutation in the Fibrinogen Bβ Chain (c.490G>A; End of Exon 3) Causes a Splicing Abnormality and Ultimately Leads to Congenital Hypofibrinogenemia (Q47120329) (← links)
• Congenital hypofibrinogenaemia: a presymptomatic detection of an extremely rare bleeding disorder in preterm twins (Q47871445) (← links)
• Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders (Q49498930) (← links)