About: JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency

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scientific article published on 01 January 2020

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) научна статия (bg) artículu científicu espublizáu en xineru de 2020 (ast) articolo scientifico (pubblicato il 2020) (it) artikull shkencor i botuar më 01 janar 2020 (sq) scientific article published on 01 January 2020 (en) article scientifique publié en 2020 (fr) im Januar 2020 veröffentlichter wissenschaftlicher Artikel (de) наукова стаття, опублікована 1 січня 2020 (uk)
publication date	wds:Q92660664-1827A85F-6E11-4D5D-A31E-AD23CDA4CE4D
publication date	2020-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q92660664-83B1837A-FAD9-48A8-943D-7C3F048FEF99
language of work or name	English
author name string	wds:Q92660664-13E26B86-E553-4EEE-9CB9-056174B45305 wds:Q92660664-1D22A1AD-4A0F-40D5-85A5-C0A2CDB51942 wds:Q92660664-2733300B-A709-40DF-BC52-14704ABA601B wds:Q92660664-2E532C1F-27AC-411A-AB4E-C882944A87A3 wds:Q92660664-39AFF35F-C556-4AE0-83C1-95D81271E301 wds:Q92660664-58266A4D-B078-44A1-A8A2-68DF8895877E wds:Q92660664-6B5D83ED-5422-455B-A50A-B4EA79DA8FDA wds:Q92660664-94BE77BC-80BB-4FF4-AC0E-DF266C5F72AC wds:Q92660664-9A39A29E-F300-4F96-B1E1-11D2448143C5 wds:Q92660664-A50455D3-7934-4770-B774-FB920EC50476 wds:Q92660664-C90D2DD4-4E0E-492C-885E-3D81B4910B6A wds:Q92660664-CE98FB71-B40B-4834-B08A-7A4DC01EAFB3 wds:Q92660664-D587D688-A39D-42B2-A201-CC1E8C5DBD1A wds:Q92660664-E746B471-18AB-49D6-8CCA-8AA7E4F7CE2A
author name string	Saleh Al-Muhsen Dusan Bogunovic Fahad A Bashiri Ayman Al-Eyadhy Hamdy H Hassan Abdullah A Alangari Areej Alkahtani Fahad Alsohime Gamal M Hasan Majed Alabdulhafid Malak Alghamdi Marta Martin-Fernandez Najla Alotaibi Sofija Buta
rdfs:label	JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency (en) JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency (nl) JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency (sq)
skos:prefLabel	JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency (en) JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency (nl) JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency (sq)
name	JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency (en) JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency (nl) JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency (sq)
author	wds:Q92660664-15A2904F-B44B-4624-974F-0D7DEEEEE930 wds:Q92660664-2DEEDFD7-5268-4888-ACFE-EEEAD96E516A wds:Q92660664-4C59F94F-4F08-459D-B293-FBBCD233E5B1 wds:Q92660664-5157DBBE-671A-4CE8-B7CE-985154DA7381 wds:Q92660664-5A5DF987-B6CC-4ED4-942B-ACD1D11F4845 wds:Q92660664-91275588-E667-4F87-86C0-70E1BFAED7C3 wds:Q92660664-965732A3-3662-42DF-B663-29C7933DEE29 wds:Q92660664-B363C883-3D18-43C6-B8EE-8F2E4B1817E2 wds:Q92660664-BC9DA6F9-2200-46A6-A2F0-E536DEEFC959 wds:Q92660664-E402D0C1-46DA-45C3-8BF5-EDFBB8CC607A
author	Jean-Laurent Casanova Emmanuelle Jouanguy Jacinta Bustamante Rabih Halwani Mohamad-Hani Temsah Zobaida Alsum Tom Le Voyer Xueer Qiu Nouf Alkhamis Conor Gruber
title	wds:Q92660664-D58B94AC-E6C1-48E8-8A43-910E78A3A6CC
title	JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency (en)
page(s)	wds:Q92660664-68CEEA38-F99F-462D-8CB8-8D5761EE8DA6
page(s)	256-265
instance of	wds:Q92660664-9B4D5F8E-2025-483F-B3CB-2D8DC12A233E
instance of	scholarly article
PubMed ID	wds:Q92660664-B72A16DD-8196-4988-9C0B-4BA94683F7BF
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/31940699
PubMed ID	31940699
published in	wds:Q92660664-5AFFC6B2-3227-47CC-9DB5-BB3B7AFEC276
published in	The New England Journal of Medicine
issue	wds:Q92660664-7322BB34-E2EC-4720-A8DD-ECC8E05E1447
volume	wds:Q92660664-A711F870-9839-4A47-9B69-83E9C31F3AAE
issue	3
volume	382
DOI	wds:Q92660664-7C01F0C1-42F8-408D-8C19-A2048365B094
DOI	http://dx.doi.org/10.1056/NEJMOA1905633
DOI	10.1056/NEJMOA1905633
PMCID	wds:Q92660664-607C9A1E-E500-4C88-9BB6-AAF5979EE97F
PMCID	7155173
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q92660664
is cites work of	Homozygous STAT2 gain-of-function mutation by loss of USP18 activity in a patient with type I interferonopathy
is cites work of	wds:Q89857650-7E6D73C0-F287-44FC-8FA0-ED8C3F3D626B

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