Hypocretin deficiency in Prader-Willi syndrome
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F05%3A00008032" target="_blank" >RIV/00216208:11110/05:00008032 - isvavai.cz</a>
Alternative codes found
RIV/00064165:_____/05:00000022 RIV/00216208:11130/05:00004182
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Hypocretin deficiency in Prader-Willi syndrome
Original language description
Prader-Willi syndrome, genetic aspects, hypocretin deficiency
Czech name
Nedostatek hypocretinu u Prader-Williho syndromu
Czech description
Prader-Williho syndrom, genetické aspekty, nedostatek hypocretinu
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/NR7916" target="_blank" >NR7916: Molecular basis of congenital microcephaly - using molecular genetics and molecular cytogenetic methods for detection of etiology of different types of microcephaly and evaluation of clinical and genetic prognosis</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
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
European Journal of Neurology
ISSN
1351-5101
e-ISSN
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Volume of the periodical
12
Issue of the periodical within the volume
1
Country of publishing house
US - UNITED STATES
Number of pages
3
Pages from-to
70-72
UT code for WoS article
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EID of the result in the Scopus database
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