Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis ; volume:7 ; number:1 ; day:16 ; month:6 ; year:2017 ; pages:1-8 ; date:12.2017
Scientific reports ; 7, Heft 1 (16.6.2017), 1-8, 12.2017

Creator: Maver, Ales
Lavtar, Polona
Ristić, Smiljana
Stopinšek, Sanja
Simčič, Saša
Hočevar, Keli
Sepčić, Juraj
Drulović, Jelena
Pekmezović, Tatjana
Novaković, Ivana
Alenka, Hodžić
Rudolf, Gorazd
Šega, Saša
Starčević-Čizmarević, Nada
Palandačić, Anja
Zamolo, Gordana
Kapović, Miljenko
Likar, Tina
Peterlin, Borut

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-017-03536-9

URN: urn:nbn:de:101:1-2019102322023102543974

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:20 AM CEST

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Associated

Maver, Ales
Lavtar, Polona
Ristić, Smiljana
Stopinšek, Sanja
Simčič, Saša
Hočevar, Keli
Sepčić, Juraj
Drulović, Jelena
Pekmezović, Tatjana
Novaković, Ivana
Alenka, Hodžić
Rudolf, Gorazd
Šega, Saša
Starčević-Čizmarević, Nada
Palandačić, Anja
Zamolo, Gordana
Kapović, Miljenko
Likar, Tina
Peterlin, Borut
SpringerLink (Online service)

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Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

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Other Objects (12)

Metabolism in presymptomatic mutation carriers of familial Amyotrophic Lateral Sclerosis

Characterization of rare germline variants in familial multiple myeloma

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Adjustment of familial relatedness in association test for rare variants

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Rare Treatments for Rare Dyslipidemias: New Perspectives in the Treatment of Homozygous Familial Hypercholesterolemia (HoFH) and Familial Chylomicronemia Syndrome (FCS)

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Adjustment of familial relatedness in association test for rare variants

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