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Factor XI deficiency, type II

MedGen UID:
543979
•Concept ID:
C0272330
•
Disease or Syndrome
SNOMED CT: Factor XI deficiency, type II (33169001)

Professional guidelines

PubMed

Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred.
Scott BT, Bovill EG, Callas PW, Hasstedt SJ, Leppert MF, Valliere JE, Varvil TS, Long GL
Thromb Haemost 2001 Jan;85(1):82-7. PMID: 11204593

Recent clinical studies

Diagnosis

Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians.
Zadra G, Asselta R, Tenchini ML, Castaman G, Seligsohn U, Mannucci PM, Duga S
Haematologica 2008 May;93(5):715-21. Epub 2008 Apr 2 doi: 10.3324/haematol.12180. PMID: 18387979

Supplemental Content

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    Practice guidelines

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