GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F05%3A00004106" target="_blank" >RIV/00216208:11130/05:00004106 - isvavai.cz</a>
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 and Degree of Hearing Loss: A Multicenter Study
Original language description
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Czech name
GJB2 mutace a stupeň ztráty sluchu: multricentrická studie
Czech description
GJB2 mutace a stupeň ztráty sluchu: multricentrická studie
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/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)
Others
Publication year
2005
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
American Journal of Human Genetics
ISSN
0002-9297
e-ISSN
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Volume of the periodical
77
Issue of the periodical within the volume
6
Country of publishing house
US - UNITED STATES
Number of pages
13
Pages from-to
945-957
UT code for WoS article
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EID of the result in the Scopus database
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