Number of the records: 1
Heterozygozity for a novel FGG Trp253Cys mutation causes hypofibrinogenaemia by specifically impairing fibrinogen secretion
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$a Vu $b D. $3 sllk_un_auth*p0047923 $4 070 $p University Medical Centre, Dept. of Genetic Medicine and Development, Geneva, Switzerland 701 -1
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Number of the records: 1