LymphedemaV1, France, Analysis, bibRecord, 000038

OL-EDA-ID Syndrome: a Novel Hypomorphic NEMO Mutation Associated with a Severe Clinical Presentation and Transient HLH

Identifieur interne : 000038 ( France/Analysis ); précédent : 000037; suivant : 000039

OL-EDA-ID Syndrome: a Novel Hypomorphic NEMO Mutation Associated with a Severe Clinical Presentation and Transient HLH

Auteurs : Silvia Ricci [Italie] ; Francesca Romano [Italie] ; Francesco Nieddu [Italie] ; Capucine Picard [États-Unis, France] ; Chiara Azzari [Italie]

Source :

Journal of Clinical Immunology [ 0271-9142 ] ; 2016.

RBID : PMC:5226985
Url:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226985

DOI: 10.1007/s10875-016-0350-x
PubMed: 27838798
PubMed Central: 5226985

Affiliations:

Links to Exploration step

PMC:5226985

Le document en format XML

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   |texte=   OL-EDA-ID Syndrome: a Novel Hypomorphic NEMO Mutation Associated with a Severe Clinical Presentation and Transient HLH
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Serveur d'exploration sur le lymphœdème

OL-EDA-ID Syndrome: a Novel Hypomorphic NEMO Mutation Associated with a Severe Clinical Presentation and Transient HLH

OL-EDA-ID Syndrome: a Novel Hypomorphic NEMO Mutation Associated with a Severe Clinical Presentation and Transient HLH

Source :

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki

	Serveur d'exploration sur le lymphœdème
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