Familial juvenile hyperuricemic nephropathy (FJHN): Localization of the gene on chromosome 16p11.2-and evidence for genetic heterogenity (3)
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064165%3A_____%2F00%3A00000003" target="_blank" >RIV/00064165:_____/00:00000003 - 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
Familial juvenile hyperuricemic nephropathy (FJHN): Localization of the gene on chromosome 16p11.2-and evidence for genetic heterogenity (3)
Original language description
Familial juvenile hyperuricemic nephropathy
Czech name
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Czech description
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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
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2000
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
2000
Issue of the periodical within the volume
66
Country of publishing house
US - UNITED STATES
Number of pages
6
Pages from-to
1989-1994
UT code for WoS article
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EID of the result in the Scopus database
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