Abnormal fibrinogen Zlín (.gamma.Thr21Ile) with missense mutation causing hypofibrinogenemia
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F14%3A00431465" target="_blank" >RIV/61389013:_____/14:00431465 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1159/000356781" target="_blank" >http://dx.doi.org/10.1159/000356781</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1159/000356781" target="_blank" >10.1159/000356781</a>
Alternative languages
Result language
angličtina
Original language name
Abnormal fibrinogen Zlín (.gamma.Thr21Ile) with missense mutation causing hypofibrinogenemia
Original language description
Hypofibrinogenemias are rare congenital disorders caused by heterozygous defects in one of the three fibrinogen genes, affecting fibrinogen synthesis, folding, assembly, and secretion. In this study we report a point mutation causing hypofibrinogenemia,fibrinogen Zlín.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
BO - Biophysics
OECD FORD branch
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Result continuities
Project
<a href="/en/project/GBP205%2F12%2FG118" target="_blank" >GBP205/12/G118: Nanobiophotonics for future health care</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2014
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Acta Haematologica
ISSN
0001-5792
e-ISSN
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Volume of the periodical
132
Issue of the periodical within the volume
2
Country of publishing house
CH - SWITZERLAND
Number of pages
4
Pages from-to
140-143
UT code for WoS article
000340514000003
EID of the result in the Scopus database
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