Fibrinogen Paris IX: a case of symptomatic hypofibrinogenemia with Bbeta Y236C and Bbeta IVS7-1G-->C mutations.

Journal of thrombosis and haemostasis : JTH

Volumn 4, Issue 5, 2006, Pages 1134-1136

  Horellou, M H ^a   Chevreaud, C ^a   Mathieux, V ^a   Conard, J ^a   de Mazancourt, P ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

FIBRINOGEN; FIBRINOGEN VARIANT; PRIMER DNA;

ADULT; CASE REPORT; CHEMICAL STRUCTURE; CHEMISTRY; FEMALE; FIBRINOGEN PARIS; GENETICS; HUMAN; LETTER; METABOLISM; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PREGNANCY; RNA SPLICING;

ADULT; BASE SEQUENCE; DNA PRIMERS; FEMALE; FIBRINOGEN; FIBRINOGENS, ABNORMAL; HUMANS; MODELS, MOLECULAR; MUTATION, MISSENSE; PREGNANCY; RNA SPLICING;

EID: 33746570000     PISSN: 15387933     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2006.01881.x     Document Type: Letter

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