Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F07%3A00008528" target="_blank" >RIV/00216208:11110/07:00008528 - isvavai.cz</a>
Alternative codes found
RIV/00064203:_____/07:1589 RIV/00216208:11130/07:1589 RIV/00064165:_____/07:00001512
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms
Original language description
Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms
Czech name
Mutační analýza MECP2 genu u slovanských pacientů s Rettovým syndromem: Nové mutace a polymorfismy
Czech description
Mutační analýza MECP2 genu u slovanských pacientů s Rettovým syndromem: Nové mutace a polymorfismy
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EB - Genetics and molecular biology
OECD FORD branch
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Result continuities
Project
<a href="/en/project/NR8355" target="_blank" >NR8355: STUDY OF MOLECULAR BASIS OF RETT SYNDROME</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach
Others
Publication year
2007
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Human Genetics
ISSN
1434-5161
e-ISSN
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Volume of the periodical
52
Issue of the periodical within the volume
4
Country of publishing house
JP - JAPAN
Number of pages
7
Pages from-to
342-348
UT code for WoS article
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EID of the result in the Scopus database
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