[Fibrinogen variation: a heterozygote dysfibrinogenemia with Arg-->His substitution in position 16 of the Aalpha chain]
Hamostaseologie
.
2002 May;22(2):7-10.
[Article in German]
Authors
H H Seydewitz
1
,
J Gram
,
H D Bruhn
,
I Witt
Affiliation
1
Universitäts-Kinderklinik Freiburg i.Br., Germany.
PMID:
12193970
No abstract available
MeSH terms
Amino Acid Substitution
Arginine
Female
Fibrinogen / genetics*
Genetic Carrier Screening
Genetic Variation*
Histidine
Humans
Male
Pedigree
Substances
fibrinogen Aalpha
Histidine
Fibrinogen
Arginine