Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F04%3A00006666" target="_blank" >RIV/00216208:11130/04:00006666 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Result language
angličtina
Original language name
Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness
Original language description
Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness
Czech name
Spektrum a frekvence mutací u GJB2 (Cx26) genu u 156 českých pacientů s peringuální hluchotou
Czech description
Spektrum a frekvence mutací u GJB2 (Cx26) genu u 156 českých pacientů s peringuální hluchotou

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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Project
<a href="/en/project/NM7417" target="_blank" >NM7417: Mutation analysis of connexin 26 gene as the most frequent cause of prelingual nonsyndromic hearing loss.</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year
2004
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Result description