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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

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    BO - Biophysics

  • OECD FORD branch

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

  • 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