Dubin-Johnson syndrome in Tunisia: Spectrum of a rare disease
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F19%3A00077669" target="_blank" >RIV/00023001:_____/19:00077669 - isvavai.cz</a>
Result on the web
<a href="https://www.sciencedirect.com/science/article/pii/S0755498218303786?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0755498218303786?via%3Dihub</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.lpm.2018.09.020" target="_blank" >10.1016/j.lpm.2018.09.020</a>
Alternative languages
Result language
angličtina
Original language name
Dubin-Johnson syndrome in Tunisia: Spectrum of a rare disease
Original language description
Dubin-Johnson syndrome (DJS) is a benign autosomal recessive disorder caused by mutations in the ATP-binding cassette subfamily C member 2 (ABCC2)/multidrug resistance-associated protein 2 (MRP2) gene that cause either absent or deficient expression of this transporter protein. This case report describes DJS in a 9-year-old boy with jaundice since childhood.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
30219 - Gastroenterology and hepatology
Result continuities
Project
—
Continuities
N - Vyzkumna aktivita podporovana z neverejnych zdroju
Others
Publication year
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Presse medicale
ISSN
0755-4982
e-ISSN
—
Volume of the periodical
48
Issue of the periodical within the volume
1
Country of publishing house
FR - FRANCE
Number of pages
2
Pages from-to
81-82
UT code for WoS article
000458896600015
EID of the result in the Scopus database
2-s2.0-85061654432