Link between a novel human gammaD-crystallin allele and a unique cataract phenotype explained by protein crystallography
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F00%3A00006090" target="_blank" >RIV/00216208:11310/00:00006090 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11110/00:00002220
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Link between a novel human gammaD-crystallin allele and a unique cataract phenotype explained by protein crystallography
Original language description
We describe a 5-years-old boy with a unique congenital cataract caused by deposition
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
<a href="/en/project/VS96141" target="_blank" >VS96141: Investigation of molecular architecture and molecular interactions of biologically important proteins and their protein domains</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)
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
Human Molecular Genetics
ISSN
0964-6906
e-ISSN
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Volume of the periodical
9
Issue of the periodical within the volume
12
Country of publishing house
GB - UNITED KINGDOM
Number of pages
8
Pages from-to
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UT code for WoS article
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EID of the result in the Scopus database
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