PD18 - Filaggrin loss-of-function variants are associated with clinical reactivity to foods

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-7022

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: PD18 - Filaggrin loss-of-function variants are associated with clinical reactivity to foods ; volume:4 ; number:1 ; day:28 ; month:2 ; year:2014 ; pages:1 ; date:3.2014
Clinical and translational allergy ; 4, Heft 1 (28.2.2014), 1, 3.2014

Creator: Van Ginkel, Dorien
Koppelman, GH
Kollen, BJ
van der Heide, S.
Kukler, J.
Flokstra-de Blok, BMJ
Dubois, AEJ

Contributor: SpringerLink (Online service)

DOI: 10.1186/2045-7022-4-S1-P18

URN: urn:nbn:de:101:1-2019102819463214926418

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

Last update: 22.11.20252025, 1:21 AM CET

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Van Ginkel, Dorien
Koppelman, GH
Kollen, BJ
van der Heide, S.
Kukler, J.
Flokstra-de Blok, BMJ
Dubois, AEJ
SpringerLink (Online service)

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PD18 - Filaggrin loss-of-function variants are associated with clinical reactivity to foods

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Other Objects (12)

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Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly

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Biallelic loss-of-function variants in GON4L cause microcephaly and brain structure abnormalities

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Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease

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Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly

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ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants

Biallelic loss-of-function variants in GON4L cause microcephaly and brain structure abnormalities

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Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings

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Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies

Novel loss-of-function variants in TRIO are associated with neurodevelopmental disorder: case report

Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease

Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease

Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly

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ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants

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Novel loss-of-function variants in TRIO are associated with neurodevelopmental disorder: case report

Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease

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