Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F05%3A00004102" target="_blank" >RIV/00216208:11130/05:00004102 - isvavai.cz</a>
Alternative codes found
RIV/00064203:_____/05:00000070
Result on the web
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DOI - Digital Object Identifier
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Result language
angličtina
Original language name
Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population
Original language description
Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population
Czech name
Dvojitá heterozygosita s mutacemi postihujícími oba GJB2 a GJB6 geny je možnou, ale velmi vzácnou příčinou vrozené hluchoty v české populaci
Czech description
Dvojitá heterozygosita s mutacemi postihujícími oba GJB2 a GJB6 geny je možnou, ale velmi vzácnou příčinou vrozené hluchoty v české populaci

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

Publication year
2005
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Result description