The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington´s disease

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F06%3A00011015" target="_blank" >RIV/00216208:11110/06:00011015 - 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

The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington´s disease

Original language description

Huntington´s disease, age-at-onset, genetic modifiers, ubiquitin carboxy-terminal hydrolase L1 (UCHL1), S18Y polymorphism

Czech name

S18Y polymorfizmus v UCHL1 genu is a genetickým modifikátorem v Huntingtonově nemoci

Czech description

Huntingtonova nemoc, Věk nástupu, Genetické modifikátory, ubiquitin carboxy-konec hydroláza L1 (UCHL1), S18Y polymorfizmus

Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

EB - Genetics and molecular biology

OECD FORD branch

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Project

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Continuities

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Publication year

2006

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Neurogenetics

ISSN

1364-6745

e-ISSN

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Volume of the periodical

7

Issue of the periodical within the volume

1

Country of publishing house

DE - GERMANY

Number of pages

4

Pages from-to

27-30

UT code for WoS article

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EID of the result in the Scopus database

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