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Title

A novel fibrinogen mutation: FGA g. 3057 C > T (p. Arg104 > Cys) impairs fibrinogen secretion

Authors
Marchi, R
Linares, M
Rojas, H
Ruiz-Sáez, A
Meyer, M
Brennan, S O
Published in BMC Hematology. 2017, vol. 17, p. 22
Abstract Abnormal fibrinogens can be caused by clinically silent hereditary mutations. A new case was detected accidentally in an 11-year-old girl when routine pre-operative coagulation tests were performed for nasal turbinate surgery.
Identifiers
PMID: 29299315
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Article (Published version) (1.6 MB) - public document Free access
Structures
Research groups Bases moléculaires des anomalies génétiques de l'hémostase (504)
Geneva Platelet Group (13)
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(ISO format)
MARCHI, R et al. A novel fibrinogen mutation: FGA g. 3057 C > T (p. Arg104 > Cys) impairs fibrinogen secretion. In: BMC Hematology, 2017, vol. 17, p. 22. https://archive-ouverte.unige.ch/unige:101804

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Deposited on : 2018-01-31

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