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GJB2 Mutations in Patients with Nonsyndromic Hearing Loss from Croatia

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064203%3A_____%2F09%3A5702" target="_blank" >RIV/00064203:_____/09:5702 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11130/09:5702

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    GJB2 Mutations in Patients with Nonsyndromic Hearing Loss from Croatia

  • Original language description

    Spectrum and frequency of mutations in the GJB2 gene in patients with non-syndromic hearing loss from Croatia is reported

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    FH - Neurology, neuro-surgery, nuero-sciences

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NR8330" target="_blank" >NR8330: Lamin A/C gene (LMNA) analysis in patients and families with autosomal recessive, axonal type of inherited neuropathy Charcot-Marie-Tooth (AR CMT2).</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2009

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Genetic Testing and Molecular Biomarkers

  • ISSN

    1945-0265

  • e-ISSN

  • Volume of the periodical

    5

  • Issue of the periodical within the volume

    13

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    7

  • Pages from-to

  • UT code for WoS article

    000270601500023

  • EID of the result in the Scopus database