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
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DOI - Digital Object Identifier
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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
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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
FH - Neurology, neuro-surgery, nuero-sciences
OECD FORD branch
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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
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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
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UT code for WoS article
000270601500023
EID of the result in the Scopus database
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