RET mutation-Tyr791Phe-the genetic cause of different diseases derived from neural crest.
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023761%3A_____%2F09%3A15" target="_blank" >RIV/00023761:_____/09:15 - 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
RET mutation-Tyr791Phe-the genetic cause of different diseases derived from neural crest.
Original language description
The aim of this study was evaluate the occurrence and genotype-phenotype correlations of the frequently discussed the Tyr791Phe mutation of the RET pproto-oncogene, detected by sequencing method in three groups of patients.
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
FB - Endocrinology, diabetology, metabolism, nutrition
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
2009
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Endocrine
ISSN
1355-008X
e-ISSN
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Volume of the periodical
36
Issue of the periodical within the volume
3
Country of publishing house
US - UNITED STATES
Number of pages
6
Pages from-to
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UT code for WoS article
000271501700011
EID of the result in the Scopus database
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