Title : Fibrinogen Kiel: a congenital dysfibrinogenaemia with (A alpha-16 Arg----His) substitution characterized by HPLC without prior isolation of fibrinogen.

Pub. Date : 1991 Aug

PMID : 1768762






1 Functional Relationships(s)
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1 A congenital fibrinogen variant in a German family is described which has been identified as a substitution of His in position 16 of the A alpha-chain for Arg, manifested over three generations in heterozygous form. Histidine fibrinogen beta chain Homo sapiens